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374073-49-1

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374073-49-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 374073-49-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,4,0,7 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 374073-49:
(8*3)+(7*7)+(6*4)+(5*0)+(4*7)+(3*3)+(2*4)+(1*9)=151
151 % 10 = 1
So 374073-49-1 is a valid CAS Registry Number.

374073-49-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethoxy-4-methoxy-2-prop-2-enylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 2-allyl-3-ethoxy-4-methoxybenzaldehyde

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:374073-49-1 SDS

374073-49-1Relevant articles and documents

Synthesis of substituted indenes from isovanillin via claisen rearrangement and ring-closing metathesis

Huang, Keng-Shiang,Wang, Eng-Chi

, p. 383 - 391 (2015/02/05)

A new synthesis of substituted indenes was studied. Based on Claisen rearrangement,Wittig reaction and ring-closing metathesis (RCM), a series of substituted indenes was synthesized from isovanillin in good yields.

Synthesis of dibenzo-fused 10-membered cyclic ethers from isovanillin Via ring-closing metathesis

Wang, Eng-Chi,Lin, Yu-Li,Chen, Hsing-Ming,Li, Sie-Rong,Kabuto, Chizuko,Takeuchi, Yoshio

, p. 125 - 136 (2007/10/03)

A synthesis of substituted dibenzo-fused 10-membered cyclic ethers is described. 2-Allylbenzyl alcohols and 2-allylphenols derived from isovanillin were coupled by the Mitsunobu reaction to construct intramolecular dienes with ether linkage. The resulting

Syntheses of substituted naphthalenes and naphthols

Huang, Keng-Shiang,Wang, Eng-Chi,Chen, Hsing-Ming

, p. 585 - 605 (2007/10/03)

Syntheses of substituted naphthalenes and naphthols are described. Based on Claisen rearrangement, ring-closing metathesis (RCM), and related reactions, isovanillin was successfully transformed into a series of substituted naphthalenes and naphthols with

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