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23427-66-9

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23427-66-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23427-66-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,4,2 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23427-66:
(7*2)+(6*3)+(5*4)+(4*2)+(3*7)+(2*6)+(1*6)=99
99 % 10 = 9
So 23427-66-9 is a valid CAS Registry Number.

23427-66-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-amino-1-methyl-5-(2-oxoethyl)cyclohexa-2,4-diene-1-carboxylate

1.2 Other means of identification

Product number -
Other names Lactamid-benzoat

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:23427-66-9 SDS

23427-66-9Relevant articles and documents

Total synthesis of myxothiazols, novel bis-thiazole β-methoxyacrylate- based anti-fungal compounds from myxobacteria

Clough, John M.,Dube, Henry,Martin, Bruce J.,Pattenden, Gerald,Reddy, K. Srinivasa,Waldron, Ian R.

, p. 2906 - 2911 (2008/02/09)

Convergent total syntheses of myxothiazols A and Z are described. The syntheses are based on elaboration of the (S)-E,E-diene thioamide 22, conversion of 22 into the bis-thiazole 27 and Wittig reactions between 27c and the aldehyde 30. The substituted β-m

Substituted 1,3-thiazole compounds, their production and use

-

, (2008/06/13)

(1) A 1,3-thiazole compound of which the 5-position is substituted with a 4-pyridyl group having a substituent including no aromatic group or (2) a 1,3-thiazole compound of which the 5-position is substituted with a pyridyl group having at the position adjacent to a nitrogen atom of the pyridyl group a substituent including no aromatic group has an excellent p38 MAP kinase inhibitory activity.

Studies on lankacidin group (T-2636) antibiotics. V. Chemical structures of lankacidin group antibiotics. (I)

Harada,Kishi

, p. 99 - 108,100, 108 (2007/10/11)

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