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7088-08-6

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7088-08-6 Usage

General Description

2,3,7,7a-Tetrahydro-7a-phenylpyrrolo[2,1-b]oxazol-5(6H)-one is a chemical compound consisting of a tetrahydro-phenylpyrrolooxazolone moiety. It is a heterocyclic compound with a pyrrolo[2,1-b]oxazolone core structure, and it is classified as a pyrrolo[2,1-b]oxazol-5(6H)-one derivative. 2,3,7,7a-Tetrahydro-7a-phenylpyrrolo[2,1-b]oxazol-5(6H)-one has potential pharmaceutical relevance due to its unique structure and potential biological activities. It may be of interest for further research and development in the fields of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 7088-08-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,8 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7088-08:
(6*7)+(5*0)+(4*8)+(3*8)+(2*0)+(1*8)=106
106 % 10 = 6
So 7088-08-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO2/c14-11-6-7-12(13(11)8-9-15-12)10-4-2-1-3-5-10/h1-5H,6-9H2

7088-08-6SDS

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 7a-phenyl-2,3,6,7-tetrahydropyrrolo[2,1-b][1,3]oxazol-5-one

1.2 Other means of identification

Product number -
Other names 7a-Phenyl-2,3,5,6,7,7a-hexahydropyrrolo(2,1-b)oxazol-5-one

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:7088-08-6 SDS

7088-08-6Downstream Products

7088-08-6Relevant articles and documents

Reaction of furan-2(3H)-ones with 1,2-binucleophiles

Amal'chieva,Egorova

, p. 1340 - 1343 (2007/10/03)

Reactions of 5-substituted furan-2(3H)-ones with ethylenediamine, 2-aminoethanol, and o-aminophenol do not stop at the stage of formation of the corresponding 4-oxoalkanoic acid amides but lead to new bi-and tricyclic structures as a result of double intr

Synthesis and central nervous system depressant activity of some bicyclic amides

Aeberli,Gogerty,Houlihan,Iorio

, p. 436 - 438 (2007/10/06)

A series of aryl bicycle analogs of succinimide and glutarimide was prepared and evaluated for CNS depressant activity. The 8a aryl 3,4,6,7,8,8a hexahydro 2H pyrrolo[2,1 b] [1,3]oxazin 6 ones possessed the best overall spectrum of activity relative to the standard agents glutethimide and phenobarbital.

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