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102975-33-7

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102975-33-7 Usage

Derivative of indole

Heterocyclic compound commonly found in natural products

Biological activities

Wide range of biological activities

Physical properties

Pale yellow solid, insoluble in water, soluble in organic solvents

Uses

Building block in the synthesis of pharmaceuticals and agrochemicals, modulation of biological processes

Potential applications

Materials science, organic electronics

Unique features

Versatile chemical compound with promising industrial and research applications

Check Digit Verification of cas no

The CAS Registry Mumber 102975-33-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,9,7 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 102975-33:
(8*1)+(7*0)+(6*2)+(5*9)+(4*7)+(3*5)+(2*3)+(1*3)=117
117 % 10 = 7
So 102975-33-7 is a valid CAS Registry Number.

102975-33-7SDS

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 1,2,4,5,6-pentamethylindole

1.2 Other means of identification

Product number -
Other names 1,2,4,5,6-Pentamethyl-1H-indole

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:102975-33-7 SDS

102975-33-7Downstream Products

102975-33-7Relevant articles and documents

SYNTHESIS OF INDOLES FROM PYRIDINIUM SALTS. 4. KETIMINES IN THE SYNTHESIS OF INDOLES FROM 3-NITROPYRIDINIUM SALTS

Yurovskaya, M. A.,Afanas'ev, A. Z.,Chertkov, V. A.,Gizatullina, E. M.,Bundel', Yu. G.

, p. 1305 - 1308 (2007/10/02)

The possibility of using certain ketimines in place of mixtures of ketone and amine in the synthesis of indoles from 3-nitropyridinium salts has been demonstrated.The use of ketimines leads, in many cases, to increased yields of indoles and simplifies their isolation.It has been established that the rate of indole formation is considerably increased in polar aprotic solvents.

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