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869287-24-1

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869287-24-1 Usage

Properties

Member of the pyrroloimidazole family
Contains a 4-fluorophenyl group
Contains a propylamino group
Contains a pyrimidinyl group
Exists in the (5S)-stereoisomeric form

Potential Pharmacological Properties

Biological activity likely due to its structure
Specific information on effects or applications not readily available

Possibility for Further Research

Potential for further research and development in pharmacology and medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 869287-24-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,2,8 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 869287-24:
(8*8)+(7*6)+(6*9)+(5*2)+(4*8)+(3*7)+(2*2)+(1*4)=231
231 % 10 = 1
So 869287-24-1 is a valid CAS Registry Number.

869287-24-1SDS

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 {(5S)-2-(4-Fluorophenyl)-3-[2-(propylamino)-4-pyrimidinyl]-6,7-di hydro-5H-pyrrolo[1,2-a]imidazol-5-yl}methanol

1.2 Other means of identification

Product number -
Other names -

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:869287-24-1 SDS

869287-24-1Downstream Products

869287-24-1Relevant articles and documents

Synthesis of potent bicyclic bisarylimidazole c-Jun N-terminal kinase inhibitors by catalytic C-H bond activation

Rech, Jason C.,Yato, Michihisa,Duckett, Derek,Ember, Brian,LoGrasso, Philip V.,Bergman, Robert G.,Ellman, Jonathan A.

, p. 490 - 491 (2007/10/03)

The efficient preparation of the privileged bicyclic bisarylimidazole kinase inhibitor scaffold was accomplished using rhodium-catalyzed C-H activation and intramolecular alkylation. The key C-H activation/alkylation step represents one of the first evalu

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