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91322-88-2

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91322-88-2 Usage

Derived from

Indole

Structure

Tetrahydro derivative (four hydrogen atoms bonded to the ring structure)

Substituent

Isopropyl group (1-methylethyl) at the first position of the ring

Potential applications

Medicinal chemistry, organic synthesis, and material science

Need for further research

To fully understand the properties and potential uses of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 91322-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,2 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91322-88:
(7*9)+(6*1)+(5*3)+(4*2)+(3*2)+(2*8)+(1*8)=122
122 % 10 = 2
So 91322-88-2 is a valid CAS Registry Number.

91322-88-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-propan-2-yl-4,5,6,7-tetrahydroindole

1.2 Other means of identification

Product number -
Other names ANBCWUXKCQDISE-UHFFFAOYSA

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:91322-88-2 SDS

91322-88-2Downstream Products

91322-88-2Relevant articles and documents

OXAZOLIDINES. 1. BASIC CATALYTIC DISPROPORTIONATION OF CYCLOHEXANOSPIRO-2-OXAZOLIDINES: SYNTHESIS OF N-SUBSTITUTED 4,5,6,7-TETRAHYDROINDOLES

Kukharev, B.F.,Stankevich, V.K.,Kukhareva, V.A.

, p. 437 - 439 (2007/10/02)

It has been shown that the basic catalytic disproportionation of cyclohexanospiro-2-oxazolidines in the presence of potasium hydroxide or sodium methylate leads to N-substituted 4,5,6,7-tetrahydroindoles with a yield of up to 73percent.The influence of the character of substituents at the nitrogen atom of oxazolidine on the course of the reaction has been established.

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