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3-Chloro-7-methoxybenzo[b]thiophene-2-carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1315550-49-2

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1315550-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1315550-49-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,5,5 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1315550-49:
(9*1)+(8*3)+(7*1)+(6*5)+(5*5)+(4*5)+(3*0)+(2*4)+(1*9)=132
132 % 10 = 2
So 1315550-49-2 is a valid CAS Registry Number.

1315550-49-2SDS

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 3-chloro-7-methoxy-1-benzothiophene-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-Chloro-7-methoxybenzo[b]thiophene-2-carbaldehyde

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:1315550-49-2 SDS

1315550-49-2Downstream Products

1315550-49-2Relevant academic research and scientific papers

Domino Vilsmeier-Haack/ring closure sequences: A facile synthesis of 3-chlorobenzo[b]thiophene-2-carbaldehydes

Paul, Nidhin,Muthusubramanian, Shanmugam

, p. 3743 - 3746 (2011)

Vilsmeier's reagent treatment of substituted diphenacyl sulfides or diphenacyl disulfides has led to the formation of a series of benzfused 3-chlorothiophene-2-carbaldehydes by a Domino Vilsmeier-Haack reaction/ring closure sequence, opening a new route for the synthesis of 3-chlorobenzo[b] thiophene-2-carbaldehydes and their benzfused analogues. A plausible mechanism has been proposed.

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