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174148-87-9

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174148-87-9 Usage

Physical State

Yellow liquid

Primary Use

Intermediate in pharmaceutical synthesis and organic compound synthesis

Other Uses

Production of dyes, perfumes, and flavoring agents

Odor

Strong

Hazard Classification

Considered hazardous; requires cautious handling

Industrial Applications

Wide range, crucial for creating various products

Check Digit Verification of cas no

The CAS Registry Mumber 174148-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,1,4 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 174148-87:
(8*1)+(7*7)+(6*4)+(5*1)+(4*4)+(3*8)+(2*8)+(1*7)=149
149 % 10 = 9
So 174148-87-9 is a valid CAS Registry Number.

174148-87-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methyl-thiophene-2,4-dicarbaldehyde

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:174148-87-9 SDS

174148-87-9Downstream Products

174148-87-9Relevant articles and documents

Synthesis and relative diatropicity of a remarkably aromatic thia[13]annulene

Mitchell, Reginald H.,Iyer, Vivekanantan S.

, p. 722 - 725 (2007/10/03)

2,4-Bis(bromomethyl)-3-methylthiophene was synthesised as an intermediate to prepare the strained thiophenobenzophanediene 11, which readily thermally valence isomerizes to the novel thia[13]annulene 10. This thia-annulene is notably diatropic and shows about 40% of the ring current of the parent bridged [14]annulene 9, which is substantially more than an analogous oxaannulene, 18, and substantially less than the azaannulene 19.

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