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74518-96-0

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74518-96-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74518-96-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,1 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74518-96:
(7*7)+(6*4)+(5*5)+(4*1)+(3*8)+(2*9)+(1*6)=150
150 % 10 = 0
So 74518-96-0 is a valid CAS Registry Number.

74518-96-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-nitro-4-(4-(trifluoromethyl)styryl)benzene

1.2 Other means of identification

Product number -
Other names -

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:74518-96-0 SDS

74518-96-0Relevant articles and documents

Microwave-assisted solvent-free synthesis of (E)-stilbenes

Wang, Liu-Chang,Li, Jiang,Zhang, Xi-Quan,Gu, Hong-Mei,Li, Bao-Lin

experimental part, p. 231 - 234 (2012/09/08)

An efficient synthesis of a series of stilbenes is reported using 4-nitrotoluene and substituted arylaldehydes as starting materials in the presence of Cs2CO3 and polyethylene glycol under solvent-free microwave irradiation. Compared with conventional method, this strategy exhibited higher stereoselectivity, shorter reaction times and has a lower environmental impact.

Metabolic N-Hydroxylation. Use of Substituent Variation to Modulate the in Vitro Bioactivation of 4-Acetamidostilbenes

Hanna, Patrick E.,Gammans, Richard E.,Sehon, Russell D.,Lee, Man-Kil

, p. 1038 - 1044 (2007/10/02)

N-Hydroxylation is an obligate step in the bioactivation of carcinogenic aryl amides.Previous reports from this laboratory demonstrated that variation of the 4' substituent of trans-4-acetamidostilbene (1) has a marked effect on the rate of its in vitro m

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