What is the 255708-80-6?

255708-80-6 is , while it's Molecular Formula is C3H7N3O3. Used in Pharmaceutical Research and Development: 255708-80-6 is used as a chiral building block for the synthesis of potential drug candidates in the pharmaceutical industry. Its chiral nature allows for the production of enantiomerically pure compounds, which are essential for ensuring the desired therapeutic effects and minimizing potential side effects. Used in the Synthesis of Enantiomerically Pure Compounds: In the field of chiral chemistry, 255708-80-6 is used as a key intermediate for the synthesis of enantiomerically pure compounds. These pure compounds are vital in pharmaceuticals, as they can exhibit different biological activities and potencies compared to their mirror-image counterparts, leading to improved efficacy and reduced side effects. Used in Drug Design and Optimization: 255708-80-6 serves as a versatile component in drug design and optimization processes. Its unique structural features and reactivity enable the development of novel drug candidates with tailored properties, such as improved pharmacokinetics, selectivity, and potency. Used in Medicinal Chemistry: In the realm of medicinal chemistry, 255708-80-6 is employed as a valuable tool for exploring the structure-activity relationships of various biologically active compounds. Its incorporation into different molecular frameworks can provide insights into the design of more effective and safer drugs. Used in Drug Manufacturing Processes: 255708-80-6 is utilized in the manufacturing processes of certain pharmaceuticals, where its unique properties contribute to the production of high-quality, enantiomerically pure drug substances.

What is the CAS number for 255708-80-6?

The CAS number of 255708-80-6 is 255708-80-6.

What is 255708-80-6 (255708-80-6) used for?

255708-80-6, also known as (R)-3-Amino-piperidine-3-carboxylic acid tert-butyl ester, is an organic compound with the molecular formula C11H22N2O2. It is a tert-butyl ester derivative of (R)-3-aminopiperidine-3-carboxylic acid and is commonly used in pharmaceutical research and development, particularly in the synthesis of potential drug candidates. As a chiral compound, it possesses a non-superimposable mirror image, making it valuable in the production of enantiomerically pure compounds, which are often crucial in pharmaceutical applications.

What is the 255708-80-6?

255708-80-6 is , while it's Molecular Formula is C3H7N3O3. Used in Pharmaceutical Research and Development: 255708-80-6 is used as a chiral building block for the synthesis of potential drug candidates in the pharmaceutical industry. Its chiral nature allows for the production of enantiomerically pure compounds, which are essential for ensuring the desired therapeutic effects and minimizing potential side effects. Used in the Synthesis of Enantiomerically Pure Compounds: In the field of chiral chemistry, 255708-80-6 is used as a key intermediate for the synthesis of enantiomerically pure compounds. These pure compounds are vital in pharmaceuticals, as they can exhibit different biological activities and potencies compared to their mirror-image counterparts, leading to improved efficacy and reduced side effects. Used in Drug Design and Optimization: 255708-80-6 serves as a versatile component in drug design and optimization processes. Its unique structural features and reactivity enable the development of novel drug candidates with tailored properties, such as improved pharmacokinetics, selectivity, and potency. Used in Medicinal Chemistry: In the realm of medicinal chemistry, 255708-80-6 is employed as a valuable tool for exploring the structure-activity relationships of various biologically active compounds. Its incorporation into different molecular frameworks can provide insights into the design of more effective and safer drugs. Used in Drug Manufacturing Processes: 255708-80-6 is utilized in the manufacturing processes of certain pharmaceuticals, where its unique properties contribute to the production of high-quality, enantiomerically pure drug substances.

What is the CAS number for 255708-80-6?

The CAS number of 255708-80-6 is 255708-80-6.

What is 255708-80-6 (255708-80-6) used for?

255708-80-6, also known as (R)-3-Amino-piperidine-3-carboxylic acid tert-butyl ester, is an organic compound with the molecular formula C11H22N2O2. It is a tert-butyl ester derivative of (R)-3-aminopiperidine-3-carboxylic acid and is commonly used in pharmaceutical research and development, particularly in the synthesis of potential drug candidates. As a chiral compound, it possesses a non-superimposable mirror image, making it valuable in the production of enantiomerically pure compounds, which are often crucial in pharmaceutical applications.

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255708-80-6

Product Name：N,O-Dimethyl-N'-Nitroso Isocyanurate
Molecular Formula：C3H7N3O3
Purity：99%
Molecular Weight：133.107

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Product Details;

CasNo： 255708-80-6

Molecular Formula： C3H7N3O3

China cas 255708-80-6 factory wholesale N,O-Dimethyl-N'-Nitroso Isocyanurate at affordable price

Molecular Formula:C3H7N3O3
Molecular Weight:133.107
PSA：79.44000
LogP:0.31400

N,O-Dimethyl-N'-nitroso isocyanurate is a chemical compound, specifically a nitrosamide. It's formed by the reaction of an amine with a nitrosating agent, and it's known to be a potential carcinogen. N,O-Dimethyl-N'-nitroso isocyanurate is also an intermediate used in the production of pesticides and pharmaceuticals.

255708-80-6 Relevant articles

A synthetic method of the dinotefuran (by machine translation)

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Paragraph 0057; 0059; 0076; 0077; 0095; 0097, (2017/08/27)

The invention discloses a method for syn...

N, O - dimethyl - N - nitro-isourea preparation method

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Paragraph 0021; 0022; 0023; 0024; 0025; 0026; 0027-0042, (2017/08/24)

The invention discloses a method for pre...

IMPROVED METHOD FOR PRODUCING NITROISOUREA DERIVATIVE

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Page/Page column 5, (2008/12/04)

Disclosed is an improved process for pro...

255708-80-6 Process route

: 57538-27-9
O-methyl-N-nitroisourea

: 74-89-5
methylamine

: 255708-80-6
N,O-dimethyl-N'-nitroisourea

Conditions

Conditions	Yield
With hydrogenchloride; sodium chloride; In water; at 40 ℃; for 6h;	95%

: C₄H₁₂N₂O₅S

: 255708-80-6
N,O-dimethyl-N'-nitroisourea

Conditions

Conditions	Yield
With sulfuric acid; nitric acid; at 25 ℃; Concentration;	43.9 g

255708-80-6 Upstream products

57538-27-9
O-methyl-N-nitroisourea
593-51-1
methylamine hydrochloride
57538-27-9
O-methyl-N-nitroisourea
74-89-5
methylamine

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