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403860-39-9

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403860-39-9 Usage

Molecular Weight

Not provided

Structure

Consists of a fluorine-substituted indan-1-ol molecule with an amino group attached to the 2-position

Physical Form

White crystalline powder

Applications

Pharmaceutical research and development
Precursor in the synthesis of various medicinal compounds
Potential biological activity studies
Reagent in organic synthesis, particularly in drug and pharmaceutical development

Check Digit Verification of cas no

The CAS Registry Mumber 403860-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,3,8,6 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 403860-39:
(8*4)+(7*0)+(6*3)+(5*8)+(4*6)+(3*0)+(2*3)+(1*9)=129
129 % 10 = 9
So 403860-39-9 is a valid CAS Registry Number.

403860-39-9SDS

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 2-amino-6-fluoro-2,3-dihydro-1H-inden-1-ol,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-Amino-6-fluoro-indan-1-ol hydrochloride

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:403860-39-9 SDS

403860-39-9Upstream product

403860-39-9Downstream Products

403860-39-9Relevant articles and documents

Bicyclic pyrrolyl amides as glucogen phosphorylase inhibitors

-

Page 59, (2010/02/06)

Heterocyclic amide derivatives, of formula (I): wherein —X-Y-Z- is selected from —S—CR4═CR5—, —CR4═CR5—S—, —O—CR4═CR5—, —CR4═CR5—O—, —N═CR4—S—, —S—CR4═N—, —NR6—CR4═CR5— and —CR4═CR5—NR6—; or a pharmaceutically acceptable salt or an in vivo hydrolysable ester thereof; (with provisos); possess glycogen phosphorylase inhibitory activity and accordingly have value in the treatment of disease states associated with increased glycogen phosphorylase activity. Processes for the manufacture of said heterocyclic amide derivatives and pharmaceutical compositions containing them are described.

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