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5H-Oxazolo[3,2-a]pyridine, hexahydro-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5632-09-7

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5632-09-7 Usage

Structure

Contains a five-membered oxazole ring fused to a six-membered pyridine ring, with a hexahydro-2-phenyl substituent (a six-membered ring with a phenyl group attached)

Potential applications

Pharmaceutical and agrochemical industries

Biological activities

Antimicrobial and antifungal properties

Check Digit Verification of cas no

The CAS Registry Mumber 5632-09-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,3 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5632-09:
(6*5)+(5*6)+(4*3)+(3*2)+(2*0)+(1*9)=87
87 % 10 = 7
So 5632-09-7 is a valid CAS Registry Number.

5632-09-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-3,5,6,7,8,8a-hexahydro-2H-[1,3]oxazolo[3,2-a]pyridine

1.2 Other means of identification

Product number -
Other names 2-Phenyl-1-oxa-indolizidin

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:5632-09-7 SDS

5632-09-7Downstream Products

5632-09-7Relevant academic research and scientific papers

Neighbour Group Participation with Reductions and Hydride Abstractions

Moehre, H.,Kamper, Ch.

, p. 512 - 520 (2007/10/02)

The reduction of N-(2-hydroxyalkyl)lactams with diisobutylaluminium hydride and the hydride ion abstraction of the corresponding amino alcohols give under neighbour group participation the fused oxazolidines.

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