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7633-56-9

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7633-56-9 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 88, p. 4061, 1966 DOI: 10.1021/ja00969a030

Check Digit Verification of cas no

The CAS Registry Mumber 7633-56-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,3 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7633-56:
(6*7)+(5*6)+(4*3)+(3*3)+(2*5)+(1*6)=109
109 % 10 = 9
So 7633-56-9 is a valid CAS Registry Number.

7633-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydroindol-1-amine

1.2 Other means of identification

Product number -
Other names 2,3-dihydro-indol-1-ylamine

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:7633-56-9 SDS

7633-56-9Relevant articles and documents

Diaza [1,4] Wittig-type rearrangement of N-allylic-N-Boc-hydrazines into γ-amino- N -Boc-enamines

Tayama, Eiji,Kobayashi, Yoshiaki,Toma, Yuka

supporting information, p. 10570 - 10573 (2016/09/02)

Diaza [1,4] Wittig-type rearrangement of N-allylic-N-Boc-hydrazines into γ-amino-N-Boc-enamines was demonstrated. The scope and limitation, experimental mechanistic studies, and a proposed reaction mechanism were also described.

3-(Hetero)aryl-4-indolylamino-α-tetralones by diastereoselective internal redox cyclization: An "azaenamine" conjugate addition

Ghavtadze, Nugzar,Narayan, Rishikesh,Wibbeling, Birgit,Wuerthwein, Ernst-Ulrich

scheme or table, p. 5185 - 5197 (2011/08/09)

(E)-3-(Hetero)aryl-1-(2-((E)-(indolin-1-ylimino)methyl)phenyl) prop-2-en-1-ones 1 undergo 6-exo-trig cyclization reactions upon treatment with BF3?Me2S in dichloromethane at low temperature to give the tetralones 10 in good yield. Th

TETRACYCLIC INDOLES AS POTASSIUM CHANNEL MODULATORS

-

Page/Page column 29, (2008/06/13)

The present invention is directed to compounds of Formula I: that are potassium channel modulators and pharmaceutical compositions thereof. The present invention is further directed to methods of treatment using the compounds and pharmaceutical compositions of the invention. The present invention is still further directed to synthetic processes for producing the compounds of the invention.

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