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101993-20-8

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101993-20-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101993-20-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,9,9 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 101993-20:
(8*1)+(7*0)+(6*1)+(5*9)+(4*9)+(3*3)+(2*2)+(1*0)=108
108 % 10 = 8
So 101993-20-8 is a valid CAS Registry Number.

101993-20-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-fluorophenyl)-5-nitro-1-benzofuran

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:101993-20-8 SDS

101993-20-8Downstream Products

101993-20-8Relevant articles and documents

Recyclable [bmIm]OH promoted one-pot heterocyclization: Synthesis of substituted benzofurans

Siddiqui,Waseem, Malik Abdul,Shamim, Shayna,Shireen,Srivastava, Arjita,Srivastava, Anjali

, p. 4154 - 4158 (2013)

A single step access to polysubstituted benzo[b]furans has been achieved under simple and eco-compatible conditions. The heterocyclization proceeded efficiently. [bmIm]OH played a triple role as a solvent, base as well as catalyst.

Sequential and one-pot reactions of phenols with bromoalkynes for the synthesis of (Z)-2-bromovinyl phenyl ethers and benzo[ b ]furans

Wang, Shihua,Li, Pinhua,Yu, Lin,Wang, Lei

supporting information; experimental part, p. 5968 - 5971 (2011/12/15)

Benzo[b]furans were prepared in one pot based on the addition/palladium- catalyzed C-H bond functionalization of phenols with bromoalkynes. The addition reactions of phenols to bromoalkynes generated (Z)-2-bromovinyl phenyl ethers in high yields with excellent regio- and stereoselectivity. The obtained (Z)-2-bromovinyl phenyl ethers subsequently proceeded by intramolecular cyclization to afford 2-substituted benzo[b]furans in good yields through palladium-catalyzed direct C-H bond functionalizations. It is important to note that the transformation of phenols with bromoalkynes into benzo[b]furans could be carried out in one pot with a simple and efficient tandem procedure.

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