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31236-61-0

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31236-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31236-61-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,2,3 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 31236-61:
(7*3)+(6*1)+(5*2)+(4*3)+(3*6)+(2*6)+(1*1)=80
80 % 10 = 0
So 31236-61-0 is a valid CAS Registry Number.

31236-61-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-N-CBZ-AMINO-CYCLOHEXANONE

1.2 Other means of identification

Product number -
Other names 1-Azetidineacetic acid,2-oxo-,phenylmethyl 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:31236-61-0 SDS

31236-61-0Relevant articles and documents

Carbazole-Containing Sulfonamides as Cryptochrome Modulators

-

Paragraph 0423-0424, (2013/11/19)

The subject matter herein is directed to carbazole-containing sulfonamide derivatives and pharmaceutically acceptable salts or hydrates thereof of structural formula I wherein the variable R1, R2, R3, R4, R5, R6, R7, A, B, C, D, E, F, G, H, a, and b are accordingly described. Also provided are pharmaceutical compositions comprising the compounds of formula I to treat a Cry-mediated disease or disorder, such as diabetes, obesity, metabolic syndrome, Cushing's syndrome, and glaucoma.

STEREOSELECTIVE SYNTHESIS OF SUBSTITUTED PIPECOLIC ACIDS

Angle, Steven R.,Arnaiz, Damian O.

, p. 515 - 518 (2007/10/02)

The stereoselective synthesis of Δ4,5-pipecolic acid derivatives is described.The key step in the sequence is a sigmatropic rearrangement.

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