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23008-85-7

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23008-85-7 Usage

Type of compound

Heterocyclic organic compound

Contains

Chlorophenyl group and an oxazolidine ring

Usage

Research and industrial applications

Synthesis building block

Pharmaceuticals and agrochemicals

Role

Chiral auxiliary in asymmetric synthesis reactions

Potential uses

Medicine and drug discovery

Unique features

Structural properties and biological activities

Check Digit Verification of cas no

The CAS Registry Mumber 23008-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,0 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23008-85:
(7*2)+(6*3)+(5*0)+(4*0)+(3*8)+(2*8)+(1*5)=77
77 % 10 = 7
So 23008-85-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H12ClNO/c1-12-6-7-13-10(12)8-2-4-9(11)5-3-8/h2-5,10H,6-7H2,1H3

23008-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenyl)-3-methyl-1,3-oxazolidine

1.2 Other means of identification

Product number -
Other names WLN: T5N COTJ A1 BR DG

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:23008-85-7 SDS

23008-85-7Relevant articles and documents

Thermal Rearrangement of some Oxazolidine N-Oxides. 2-Alkyl-6-aryl-3,4-dihydro-2H-1,5,2-dioxazines

Saba, Shahrokh,Domkowski, Patrick W.,Firooznia, Fariborz

, p. 921 - 923 (2007/10/02)

3-Alkyl-2-aryloxazolidines are oxidized with 3-chloroperoxybenzoic acid to produce the corresponding oxazolidine N-oxides.These N-oxides undergo thermal rearrangement to give 2-alkyl-6-aryl-3,4-dihydro-2H-1,5,2-dioxazines in 55-85 percent yield.

New compounds: Oxazolidines and derived amino alcohols.

Ager,May

, p. 499 - 500 (2007/10/05)

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