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215597-35-6

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215597-35-6 Usage

General Description

1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER, also known as methyl 1-aminocyclobutane-1-carboxylate, is a chemical compound with the molecular formula C6H11NO2. It is a methyl ester derivative of 1-aminocyclobutane-1-carboxylic acid, which is a cyclic non-proteinogenic amino acid. 1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER is used in organic synthesis and pharmaceutical research as a building block for the synthesis of various biologically active molecules. It has potential applications in the development of new drugs and pharmaceuticals due to its unique structural properties and potential biological activity. However, its use and handling should be carried out with appropriate precautions and under the guidance of trained professionals due to its potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 215597-35-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,5,9 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 215597-35:
(8*2)+(7*1)+(6*5)+(5*5)+(4*9)+(3*7)+(2*3)+(1*5)=146
146 % 10 = 6
So 215597-35-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO2.ClH/c1-9-5(8)6(7)3-2-4-6;/h2-4,7H2,1H3;1H

215597-35-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1-aminocyclobutane-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-aminocyclobutyl carboxylic acid methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:215597-35-6 SDS

215597-35-6Relevant articles and documents

UREA DERIVATIVES AS PYRUVATE KINASE ACTIVATORS

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Paragraph 472-474, (2022/02/15)

The subject matter described herein is directed to pyruvate kinase activating compounds of Formula I and pharmaceutical salts thereof, methods of preparing the compounds, pharmaceutical compositions comprising the compounds and methods of administering the compounds for the treatment of diseases associated with PKR and/or PKM2, such as pyruvate kinase deficiency, sickle cell disease, and beta-thalassemia.

Substituted Pyrimidine and Triazine Compounds

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Page/Page column 34, (2010/07/10)

Substituted pyrimidine and triazine compounds corresponding to formula I wherein R1, R2, R3, R4a, R4b, R5a, R5b, R7, R8, R9a, R9b, R10, R11, A, a, b, s, t, V, W1, W2 and W3 have defined meanings, pharmaceutical compositions comprising such compounds, a process for preparing such compounds, and the use of such compounds and compositions to treat or inhibit pain and/or other disorders or disease states.

A novel synthesis, including asymmetric synthesis, of α-quaternary α-amino acid methyl esters from ketones via sulfinyloxiranes

Satoh, Tsuyoshi,Hirano, Mizue,Kuroiwa, Akio

, p. 2659 - 2662 (2007/10/03)

Sulfinyloxiranes were synthesized from ketones and chloromethyl p-tolyl sulfoxide in two steps in almost quantitative yields. The sulfinyloxiranes were treated with NaN3 in the presence of NH4Cl to afford α-azido aldehydes, which wer

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