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15177-34-1

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15177-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15177-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,7 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15177-34:
(7*1)+(6*5)+(5*1)+(4*7)+(3*7)+(2*3)+(1*4)=101
101 % 10 = 1
So 15177-34-1 is a valid CAS Registry Number.

15177-34-1SDS

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 N-hydroxybenzenecarbothioamide

1.2 Other means of identification

Product number -
Other names thiobenzhydroxamic acid

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:15177-34-1 SDS

15177-34-1Relevant articles and documents

N–hydroxybenzothioamide derivatives as green and efficient corrosion inhibitors for mild steel: Experimental, DFT and MC simulation approach

Alqahtani, Mohammed S.,Asatkar, Ashish,Berdimurodov, Elyor,Haldhar, Rajesh,Kaya, Sava?,Kazi, Mohsin,Salim, Rajae,Syed, Rabbani,Verma, Dakeshwar Kumar

, (2021/05/26)

In this research work, the thiohydroxamic acid derivatives included N–hydroxybenzothioamide (THA–H), 4–bromo–N–hydroxybenzothioamide (THA–Br), and 4–methoxy–N–hydroxybenzothioamide (THA–OCH3) were first introduced as effective and green corrosi

Collision-induced dissociation mass spectra of glucosinolate anions

Bialecki, Jason B.,Ruzicka, Josef,Weisbecker, Carl S.,Haribal, Meena,Attygalle, Athula B.

experimental part, p. 272 - 283 (2010/08/19)

Collision-induced dissociation (CID)mass spectra of differently substituted glucosinolates were investigated under negative-ion mode. Data obtained from several glucosinolates and their isotopologues (34S and 2H) revealed that many p

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