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Cyclopent[e]-1,3-oxazin-2(3H)-one, hexahydro-4-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122797-14-2

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122797-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122797-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,7,9 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 122797-14:
(8*1)+(7*2)+(6*2)+(5*7)+(4*9)+(3*7)+(2*1)+(1*4)=132
132 % 10 = 2
So 122797-14-2 is a valid CAS Registry Number.

122797-14-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methyl-hexahydro-cyclopenta[e][1,3]oxazin-2-one

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:122797-14-2 SDS

122797-14-2Downstream Products

122797-14-2Relevant academic research and scientific papers

DIASTEREOSELECTIVITY IN THE ADDITION OF ENOLATE ANIONS TO N-METHOXYCARBONYLIMINES GENERATED IN SITU FROM α-METHOXY CARBAMATES

Shono, Tatsuya,Kise, Naoki,Sanda, Fumio,Ohi, Satoru,Yoshioka, Ken

, p. 1253 - 1256 (2007/10/02)

The diastereoselectivity of the addition of enolate anions of ketones or esters to N-Methoxycarbonylimines generated in situ from α-Methoxy carbamates was studied.

Syntheses via Isoxazolines, 6. - Asymmetric Induction in the Reduction of 2-Isoxazolines to Yield γ-Amino Alcohols with Two or Three Vicinal Stereocentres

Jaeger, Volker,Buss, Volker,Schwab, Wilfried

, p. 122 - 139 (2007/10/02)

The substituted 3-aminopropanols 3 and 5 with two or three adjacent chiral centres are prepared from alkenes and nitrile oxides via LiAlH4 reduction of intermediate isoxazolines 2 and 4, respectively, in a regio- and stereoselective mode. 4-Alkyl groups g

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