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825-70-7

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825-70-7 Usage

General Description

5-Fluoro-2,3-dihydro-2-Methyl-1H-Indole is a chemical compound with a fluorine atom attached to a dihydro-2-Methyl-1H-Indole core. It is a white to off-white solid with a molecular formula C9H10FIN and a molecular weight of 261.08 g/mol. 5-fluoro-2,3-dihydro-2-Methyl-1H-Indole may be used in various research and industrial applications, including pharmaceuticals, agrochemicals, and materials science. Its specific properties and potential uses are subject to ongoing research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 825-70-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 825-70:
(5*8)+(4*2)+(3*5)+(2*7)+(1*0)=77
77 % 10 = 7
So 825-70-7 is a valid CAS Registry Number.

825-70-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-fluoro-2-methyl-2,3-dihydro-1H-indole

1.2 Other means of identification

Product number -
Other names 5-fluoro-2-methylindoline

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:825-70-7 SDS

825-70-7Downstream Products

825-70-7Relevant articles and documents

METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND, AND NOVEL METAL-DIAMINE COMPLEX

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Paragraph 0306; 0307, (2016/12/22)

The present invention pertains to a method for producing an optically active compound which includes a step for reducing an imino group of an imine compound or a step for reducing an unsaturated bond of a heterocyclic compound, while in the presence of hydrogen gas as a hydrogen donor and one or more types of complexes selected from a group consisting of a complex represented by general formula (1), a complex represented by general formula (2), a complex represented by general formula (3), and a complex represented by general formula (4) (the general formulas (1)-(4) are as stipulated by claim 1).

NOVEL PYRIMIDINE DERIVATIVES, PREPARATION THEREOF, AND PHARMACEUTICAL USE THEREOF AS AKT(PKB) PHOSPHORYLATION INHIBITORS

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Paragraph 1216-1220, (2013/10/22)

The present invention relates to novel chemical compounds derived from pyrimidines, to the method for preparing same, to the novel intermediates obtained, to the use thereof as drugs, to the pharmaceutical compositions containing same, and to the therapeutic use thereof as AKT inhibitors.

Chemoenzymatic preparation of optically active secondary amines: a new efficient route to enantiomerically pure indolines

Gotor-Fernandez, Vicente,Fernandez-Torres, Pedro,Gotor, Vicente

, p. 2558 - 2564 (2007/10/03)

An efficient chemoenzymatic route for the synthesis of optically active substituted indolines has been developed. Different lipases have been tested in the alkoxycarbonylation of these secondary amines, Candida antarctica lipase A (CAL-A) was found to be the best biocatalyst for 2-substituted-indolines, and C. antarctica lipase B (CAL-B) for 3-methylindoline. The combination of lipases with a variety of allyl carbonates and tert-butyl methyl ether (TBME) as solvent has allowed the isolation of the carbamate and amine derivatives with a high level of enantiopurity.

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