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61638-04-8

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61638-04-8 Usage

Chemical class

Thioether

Derivative of

Benzene

Common uses

Synthesis of pharmaceuticals
Synthesis of agricultural chemicals
Intermediate in production of insecticides and herbicides

Potential applications

Antitumor agent (inhibits cancer cell growth)

Hazardous nature

Considered a hazardous chemical

Handling precautions

Should be handled with caution in a controlled laboratory setting

Check Digit Verification of cas no

The CAS Registry Mumber 61638-04-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,3 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61638-04:
(7*6)+(6*1)+(5*6)+(4*3)+(3*8)+(2*0)+(1*4)=118
118 % 10 = 8
So 61638-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3S/c1-12-8-5-10(14-3)9(13-2)4-7(8)6-11/h4-6H,1-3H3

61638-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dimethoxy-4-methylsulfanylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 2,5-Dimethoxy-4-methylthiobenzaldehyd

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:61638-04-8 SDS

61638-04-8Relevant articles and documents

Accelerated Fmoc solid-phase synthesis of peptides with aggregation-disrupting backbones

Huang, Yi-Chao,Guan, Chao-Jian,Tan, Xiang-Long,Chen, Chen-Chen,Guo, Qing-Xiang,Li, Yi-Ming

supporting information, p. 1500 - 1506 (2015/01/30)

In this work, we describe an accelerated solid-phase synthetic protocol for ordinary or difficult peptides involving air-bath heating and amide protection. For the Hmsb-based backbone amide protection, an optimized acyl shift condition using 1,4-dioxane w

FACILE SYNTHESIS OF ALKYLTHIOBENZALDEHYDES

Schwartz, John A.

, p. 565 - 570 (2007/10/02)

Alkoxyl alkylthiobenzaldehydes can be readily prepared from the corresponding bromobenzaldehydes and the sodium salt of primary mercaptanes in DMF.

Monomethylthio analogues of 1-(2,4,5-trimethoxyphenyl)-2-aminopropane

Jacob III,Anderson III,Meshul,Shulgin,Castagnoli Jr.

, p. 1235 - 1239 (2007/10/06)

Regiospecific syntheses of the three monomethylthio analogues of 1-(2,4,5- trimethoxyphenyl)-2-aminopropane are described. The three isomeric amines were evaluated for potential psychotomimetic potency using the rabbit hyperthermia assay. Enantiomeric com

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