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32787-80-7

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32787-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32787-80-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,8 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 32787-80:
(7*3)+(6*2)+(5*7)+(4*8)+(3*7)+(2*8)+(1*0)=137
137 % 10 = 7
So 32787-80-7 is a valid CAS Registry Number.

32787-80-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-(3-nitrophenyl)-N-(4H-1,2,4-triazol-4-yl)methanimine

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:32787-80-7 SDS

32787-80-7Relevant articles and documents

Syntheses, in vitro α-amylase and α-glucosidase dual inhibitory activities of 4-amino-1,2,4-triazole derivatives their molecular docking and kinetic studies

Aboaba, Sherifat A.,Chigurupati, Sridevi,Hameed, Shehryar,Kannan Maharajan, Mari,Kanwal,Mohammed Khan, Khalid.,Perveen, Shahnaz,Shamim, Shahbaz,Taha, Muhammad,Ur Rehman, Ashfaq,Wadood, Abdul,Yeye, Emmanuel Oloruntoba

, (2020/04/23)

Thirty-three 4-amino-1,2,4-triazole derivatives 1–33 were synthesized by reacting 4-amino-1,2,4-triazole with a variety of benzaldehydes. The synthetic molecules were characterized via 1H NMR and EI-MS spectroscopic techniques and evaluated for

REACTION OF SCHIFF BASES OBTAINED FROM 4-AMINOANTIPYRINE AND 4-AMINO-1,2,4-TRIAZOLE WITH KETONES

Letunov, V. I.

, p. 145 - 149 (2007/10/02)

With acetophenone and p-nitroacetophenone in alcohol and benzene media in the presence of acid N-arylidene-4-aminoantipyrines form α,β-unsaturated ketones, and with antipyrine the form aryldiantipyrylmethanes.With the same ketones N-arylidene-4-amino-1,2,4-triazoles form the products from addition at the azomethine bond.In both cases reaction with benzylideneacetone was not detected.

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