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1H-Indene, 1-methyl-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1004-63-3

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1004-63-3 Usage

Chiral compound

Has a non-superimposable mirror image

(S)-enantiomer

The specific configuration of the compound

Used in production of pharmaceuticals

Due to its unique structure and reactivity

Utilized in synthesis of organic compounds

For the creation of various compounds

Intermediate in manufacturing of fragrances and flavors

As a starting material in the synthesis of these products

Potential applications in materials science and nanotechnology

Due to its interesting properties, it has been studied for use in these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1004-63-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1004-63:
(6*1)+(5*0)+(4*0)+(3*4)+(2*6)+(1*3)=33
33 % 10 = 3
So 1004-63-3 is a valid CAS Registry Number.

1004-63-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S)-1-methyl-1H-indene

1.2 Other means of identification

Product number -
Other names (+)-(S)-1-Methylindene

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:1004-63-3 SDS

1004-63-3Upstream product

1004-63-3Downstream Products

1004-63-3Relevant academic research and scientific papers

Mn-salen catalyzed asymmetric epoxidation of (±)-3-alkylindene: Reagent-dependent stereoselectivity

Noguchi, Yukiko,Irie, Ryo,Fukuda, Tsutomu,Katsuki, Tsutomu

, p. 4533 - 4536 (1996)

Epoxidation of (±)-3-alkylindenes was examined with various (salen)manganese(III) complexes as catalysts and, from the analysis of the obtained data, it was found that the location and nature of C3- and C3'- substituents of the Mn-catalysts strongly influenced the stereochemistry of the epoxidation.

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