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100278-39-5

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100278-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100278-39-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,2,7 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100278-39:
(8*1)+(7*0)+(6*0)+(5*2)+(4*7)+(3*8)+(2*3)+(1*9)=85
85 % 10 = 5
So 100278-39-5 is a valid CAS Registry Number.

100278-39-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,5-trimethoxy-N-[4-[[(E)-(2-nitrophenyl)methylideneamino]carbamoyl]phenyl]benzamide

1.2 Other means of identification

Product number -
Other names BENZOIC ACID,p-(3,4,5-TRIMETHOXYBENZAMIDO)-,2-(o-NITROBENZYLIDENE)HYDRAZIDE

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:100278-39-5 SDS

100278-39-5Downstream Products

100278-39-5Relevant articles and documents

Studies on thiazolidin-4-ones: Part XX-synthesis and antimicrobial activity of 2-aryl-5H/methyl/carboxymethyl-3-[4-(3,4,5-trimethoxybenzamido)-benzoylamino] thiazolidin-4-ones

Joshi, Nailesh,Patel, Pankaj,Parekh, Hansa

, p. 867 - 870 (2007/10/03)

2-Aryl-5-H/methyl/carboxymethyl-3-[4-(3,4,5-trimethoxybenzamido) benzoylamino]thiazolidin-4-ones (3a-m, 4a-m and 5a-m) have been synthesised by the cyclocondensation of thioglycolic acid/thiolactic acid/thiomalic acid with N-substituted benzal-4-(3,4,5-trimethoxybenzamido)benzoylhydrazines (2a-m) which in turn are prepared by the action of aryldehydes on 4-(3,4,5-trimethoxybenzamido)benzoylhydrazide (1). The structures of the compounds 2a-m, 3a-m and 5a-m have been confirmed from elemental analysis, IR, 1H NMR and mass spectral data. All the products are evaluated for their in vitro growth inhibitory activity against several microbes like S. aureus, S. pyogens, E. coli, K. arogens and A. niger.

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