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Acetamide, N-[2-(2,3-dihydro-2-oxo-1H-indol-3-yl)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70638-13-0

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70638-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70638-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,3 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70638-13:
(7*7)+(6*0)+(5*6)+(4*3)+(3*8)+(2*1)+(1*3)=120
120 % 10 = 0
So 70638-13-0 is a valid CAS Registry Number.

70638-13-0SDS

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 N-[2-(2-oxo-1,3-dihydroindol-3-yl)ethyl]acetamide

1.2 Other means of identification

Product number -
Other names N(b)-Acetyl-2-oxo-2,3-dihydrotryptamin

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:70638-13-0 SDS

70638-13-0Downstream Products

70638-13-0Relevant academic research and scientific papers

Novel formations of 6-mesyloxytryptamines and 1-substituted 3a-(4- chlorobutoxy)-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indoles in the reaction of nb-substituted 1-hydroxytryptamines with mesyl chloride

Hasegawa, Masakazu,Nagahama, Yoshiyuki,Kobayashi, Kensuke,Hayashi, Masumi,Somei, Masanori

, p. 483 - 491 (2007/10/03)

Formations of 6-mesyloxytryptamines and 1-substituted 3a-(4- chlorobutoxy)-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indoles were newly found in the reactions of Nb-substituted 1-hydroxytryptamines with mesyl chloride in THF. The latter compounds suggest that

Reactions of 1-hydroxyindoles with p-toluenesulfonyl chloride and p-toluenesulfonic acid

Somei, Masanori,Yamada, Fumio,Goto, Aya,Hayashi, Masumi,Hasegawa, Masakazu

, p. 2487 - 2497 (2007/10/03)

1-Hydroxyindoles produced novel types of compounds such as 4-substituted indoles and 4H-1,3-dioxolo[4,5-b]indoles upon reaction with p-toluenesulfonyl chloride in acetone. Contrastively, 5-tosyloxyindole and 2H-1,2-oxazino[2,3-a]indole were generated upon reaction with p-toluenesulfonic acid in acetone.

A novel methodology for preparing 5-chloro- and 5-bromotryptamines and tryptophans, and its application to the synthesis of (±)-bromochelonin B

Hasegawa, Masakazu,Yamada, Koji,Nagahama, Yoshiyuki,Somei, Masanori

, p. 2815 - 2821 (2007/10/03)

A novel methodology for introducing chlorine or bromine into the 5- position of tryptamines was found through 1-hydroxytryptamines. The chemistry was applied to the syntheses of (±)-5-chloro-, -5-bromotryptophan derivatives, and (±)-bromochelonin B.

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