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13980-78-4

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13980-78-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13980-78-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,8 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13980-78:
(7*1)+(6*3)+(5*9)+(4*8)+(3*0)+(2*7)+(1*8)=124
124 % 10 = 4
So 13980-78-4 is a valid CAS Registry Number.

13980-78-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(1-phenyltetrazol-5-yl)sulfanylacetate

1.2 Other means of identification

Product number -
Other names F0835-0010

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:13980-78-4 SDS

13980-78-4Relevant articles and documents

Electrolytic partial fluorination of organic compounds. 89: Regioselective anodic fluorination of tetrazolyl sulfides

Zagipa, Bakenova,Nagura, Hirokatsu,Fuchigami, Toshio

, p. 1168 - 1173 (2007)

Anodic fluorination of five-membered nitrogen-containing heterocyclic sulfides like tetrazolyl sulfides was comparatively studied. The anodic fluorination of tetrazolyl sulfides having α-electron-withdrawing groups was successfully carried out to provide

Synthesis and evaluation of tetrazole-based hydrazone derivatives bearing a pyridine moiety as antimicrobial agents

?zdemir, Ahmet,Altintop, Mehlika Dilek,Sever, Belgin,Cantürk, Zerrin,Kaplancikli, Zafer Asim

, p. 687 - 693 (2015/09/01)

2-[(1-Methyl/Phenyl-1 H-tetrazol-5-yl)thio]-N '-[(aryl)methylidene/ethylidene]acetohydrazides were synthesized and investigated in vitro against pathogenic bacteria and Candida species for their antimicrobial activity using CLSI broth microdilution method

Synthesis and bioactivity of 5-(1-aryl-1H-tetrazol-5-ylsulfanylmethyl)-N- xylopyranosyl-1,3,4-oxa(thia)diazol-2-amines

He, Yao-Wu,Cao, Ling-Hua,Zhang, Jian-Bin,Wang, Duo-Zhi,Aisa, Haji Akber

scheme or table, p. 551 - 559 (2011/04/27)

A series of new N′-[N-(2,3,4-tri-O-acetyl-β-d-xylopyranosyl) thiocarbamoyl]-2-[(1-aryl-1H-tetrazol-5-yl)sulfanyl]acetohydrazides 5a-5e were synthesized rapidly in high yields from 2-(1-aryl-1H-tetrazol-5-ylsulfanyl) acetohydrazides 3a-3e and 2,3,4-tri-O-a

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