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180624-15-1

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180624-15-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 180624-15-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,6,2 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 180624-15:
(8*1)+(7*8)+(6*0)+(5*6)+(4*2)+(3*4)+(2*1)+(1*5)=121
121 % 10 = 1
So 180624-15-1 is a valid CAS Registry Number.

180624-15-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-2-((trimethylsilyl)ethynyl)aniline

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:180624-15-1 SDS

180624-15-1Relevant articles and documents

2,3-Difunctionalized Indoles via Radical Acylation or Trifluoromethylation of ortho-Alkynylphenyl Isonitriles

Leifert, Dirk,Weidlich, Frauke,Adler, Florin,Daniliuc, Constantin G.,Alasmary, Fatmah A.,Studer, Armido

supporting information, p. 284 - 288 (2021/12/27)

A radical cascade to 2,3-disubstituted indoles proceeding via acylation or trifluoromethylation of ortho-alkynylphenyl isonitriles is presented. In these cascades, two C–C bonds and one C–O bond are formed using an inexpensive oxidant and a catalytic copp

Copper-Catalyzed Enantioselective C-H Arylation between 2-Arylindoles and Hypervalent Iodine Reagents

Liang, Hao,Zhu, Guoxun,Pu, Xiaoyun,Qiu, Liqin

supporting information, p. 9246 - 9250 (2021/12/06)

The copper-catalyzed enantioselective C-H arylation between 2-arylindoles and hypervalent iodine reagents has been successfully developed, which provides a convenient and economical route to the highly atroposelective synthesis of axially chiral indole de

Photocatalytic Biheterocyclization of 1,7-Diynes for Accessing Skeletally Diverse Tricyclic 2-Pyranones

Wang, Lu,Xu, Ting,Rao, Qian,Zhang, Tian-Shu,Hao, Wen-Juan,Tu, Shu-Jiang,Jiang, Bo

supporting information, p. 7845 - 7850 (2021/10/20)

A new and green route to skeletally diverse oxo-heterocyclic architectures such as pyrano[3,4-c]chromen-2-ones and pyrano[3,4-c]quinolin-2-ones is reported via an unprecedented photocatalytic Kharasch-type cyclization/1,5-(SN″)-substitution/elimination/6π

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