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24254-61-3

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24254-61-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24254-61-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,5 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24254-61:
(7*2)+(6*4)+(5*2)+(4*5)+(3*4)+(2*6)+(1*1)=93
93 % 10 = 3
So 24254-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO4/c1-8(7-11(13)16-2)9-3-5-10(6-4-9)12(14)15/h3-6,8H,7H2,1-2H3

24254-61-3SDS

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 methyl 3-(4-nitrophenyl)butanoate

1.2 Other means of identification

Product number -
Other names 3-(4-Nitrophenyl)butanoic 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:24254-61-3 SDS

24254-61-3Upstream product

24254-61-3Relevant articles and documents

Pyrimidinedione derivatives and antiarrythmic agents containing the same

-

, (2008/06/13)

A pyrimidinedione derivative compound has a basic backbone in which a phenyl group part and a pyrimidinedione part are linked by a linking structure comprising an alkyl chain containing two nitrogen atoms. This linking structure is represented by STR1 [wherein A is --(CH2)n --, --CO-- or --O--(CH2)m --; each of R1 and R2 is independently a hydrogen atom or a lower alkyl group which may be substituted by a hydroxyl group, or R1 and R2 may be so linked with each other as to make an alkylene chain and thus form a heterocyclic structure; R5 is a halogen atom, a hydroxyl group, a lower alkyloxycarbonyl group, a lower alkyloxy group which may be substituted by a lower alkyloxy group, or a lower alkyl group which may be substituted by a hydroxyl group, or R5 may be so linked with R1 as to make an alkylene chain and thus form a heterocyclic structure; n is 0, 1, 2 or 3 (when R5 is the hydroxyl group, n≠0); m is 0, 1, 2 or 3; and k is 0, 1, 2 or 3 (however, a compound in which A is --O--(CH2)m -- and R5 is the hydroxyl group is excluded from the pyrimidinedione derivative)]. The pyrimidinedione derivative and its acid addition salt are useful for a medical treatment of cardiac arrhythmias.

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