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141738-80-9

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141738-80-9 Usage

Chemical Properties

Colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 141738-80-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,7,3 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141738-80:
(8*1)+(7*4)+(6*1)+(5*7)+(4*3)+(3*8)+(2*8)+(1*0)=129
129 % 10 = 9
So 141738-80-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H3ClF3I/c8-5-3-4(7(9,10)11)1-2-6(5)12/h1-3H

141738-80-9 Well-known Company Product Price

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  • Alfa Aesar

  • (A14685)  3-Chloro-4-iodobenzotrifluoride, 98%   

  • 141738-80-9

  • 1g

  • 589.0CNY

  • Detail
  • Alfa Aesar

  • (A14685)  3-Chloro-4-iodobenzotrifluoride, 98%   

  • 141738-80-9

  • 5g

  • 1622.0CNY

  • Detail
  • Alfa Aesar

  • (A14685)  3-Chloro-4-iodobenzotrifluoride, 98%   

  • 141738-80-9

  • 25g

  • 6893.0CNY

  • Detail

141738-80-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-CHLORO-4-IODOBENZOTRIFLUORIDE

1.2 Other means of identification

Product number -
Other names 2-chloro-1-iodo-4-(trifluoromethyl)benzene

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:141738-80-9 SDS

141738-80-9Upstream product

141738-80-9Relevant articles and documents

Conversion of aromatic amino into trifluoromethyl groups through a Sandmeyer-type transformation

Wang, Xi,Xu, Yan,Zhou, Yujing,Zhang, Yan,Wang, Jianbo

supporting information, p. 2143 - 2148 (2014/08/18)

A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups via a Sandmeyer-type reaction is reported. The transformation involves diazotization of the aromatic amines with tert-butyl nitrite and hydrochloric acid to form aryldiazonium chlorides, followed by trifluoromethylation with trifluoromethylsilver at low temperature. Various readily available aromatic amines are smoothly converted under mild conditions. Georg Thieme Verlag Stuttgart. New York.

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