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56632-33-8

56632-33-8

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56632-33-8 Usage

Structure

A derivative of 1H-indole-1-carboxamide in a dihydro form

Appearance

White to light yellow solid

Molecular weight

175.19 g/mol

Usage

Research and development of pharmaceuticals, intermediate in organic synthesis

Potential applications

Therapeutic uses, building block in the synthesis of more complex molecules and pharmaceutical compounds

Precise properties

Not extensively studied

Check Digit Verification of cas no

The CAS Registry Mumber 56632-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,3 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56632-33:
(7*5)+(6*6)+(5*6)+(4*3)+(3*2)+(2*3)+(1*3)=128
128 % 10 = 8
So 56632-33-8 is a valid CAS Registry Number.

56632-33-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Indolinecarboxamide

1.2 Other means of identification

Product number -
Other names 1-carbamoyl-thio carbonohydrazide

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:56632-33-8 SDS

56632-33-8Downstream Products

56632-33-8Relevant articles and documents

6-HETEROCYCLIC-4-AMINO-1,2,2A,3,4,5-HEXAHYDROBENZ[CD]INDOLES

-

, (2008/06/13)

6-Heterocyclic-4-amino-l,2,2a,3,4,5-hexahydrobenz[cd]indoles are provided which are useful in modifying the function of serotonin in mammals.

6-heterocyclic-4-amino-1,2,2a,3,4,5-hexahydrobenz(cd)indoles and pharmaceutical use thereof

-

, (2008/06/13)

6-Heterocyclic-4-amino-1,2,2a,3,4,5-hexahydrobenz[cd]indoles are provided which are useful in modifying the function of serotonin in mammals.

Some Extensions of von Braun (BrCN) Reaction on Organic Bases, Part IV

Siddiqui, Salimuzzaman,Haider, S. Imtiaz,Ahmad, S. Salman,Siddiqui, B. Shaheen

, p. 546 - 549 (2007/10/02)

Extensions of von Braun cyanogen bromide reaction have been undertaken on some aliphatic and heterocyclic amines.Monocyanamides of all these bases yielded their respective urea and carboxamide derivatives on hydrolysis with dilute hydrochloric acid.They also gave the amido derivatives on reaction with Zn/HCl, as in the case of diisobutyl and di-2-butyl cyanamides. - Key words: von Braun Cyanogen Bromide Reaction

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