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3-Cyclohexene-1-carboxylic acid, 3-methyl-6-[(2-oxo-3-oxazolidinyl)carbonyl]-, methyl ester, (1R,6R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116733-44-9

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116733-44-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116733-44-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,7,3 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 116733-44:
(8*1)+(7*1)+(6*6)+(5*7)+(4*3)+(3*3)+(2*4)+(1*4)=119
119 % 10 = 9
So 116733-44-9 is a valid CAS Registry Number.

116733-44-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-{[(4'R,5'R)-1'-Methyl-5'-(methoxycarbonyl)cyclohexen-4'-yl]-carbonyl}-1,3-oxazolidin-2-one

1.2 Other means of identification

Product number -
Other names (1R,6R)-3-Methyl-6-(2-oxo-oxazolidine-3-carbonyl)-cyclohex-3-enecarboxylic acid methyl ester

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:116733-44-9 SDS

116733-44-9Downstream Products

116733-44-9Relevant academic research and scientific papers

Bis(oxazoline) derived cationic aqua complexes: Highly effective catalysts for enantioselective Diels-Alder reactions

Ghosh, Arun K.,Cho, Hanna,Cappiello, John

, p. 3687 - 3691 (1998)

Cationic aqua complex derived from bidentate inda-box ligand and Cu(ClO4)2·6H2O is an excellent catalyst (5-10 mol%) for enantioselective (92-99% ee) Diels-Alder reactions of cyclopentadiene and various bidentate dienophil

Characterization of the Chiral Titanium Reagent Prepared from the Tartrate-derived Chiral Diol and Titanium Dichloride Diisopropoxide

Iwasawa, Nobuharu,Hayashi, Yujiro,Sakurai, Hidehiro,Narasaka, Koichi

, p. 1581 - 1584 (2007/10/02)

The chiral titanium reagent prepared from the tartrate-derived chiral 1,4-diol and titanium dichloride diisopropoxide was characterized based on the NMR and experimental analyses.

Asymmetric Diels-Alder Reaction Catalyzed by a Chiral Titanium Reagent

Narasaka, Koichi,Iwasawa, Nobuharu,Inoue, Masayuki,Yamada, Tohru,Nakashima, Masako,Sugimori, Jun

, p. 5340 - 5345 (2007/10/02)

A highly enantioselective Diels-Alder reaction has been developed by employing a chiral titanium reagent generated in situ from dichlorodiisopropoxytitanium and the chiral diol 1d, which is easily derived from tartaric acid.With a catalytic amount of the

Asymmetric Diels-Alder Reaction by the Use of a Chiral Titanium Catalyst with Molecular Sieves 4A. Remarkable Solvent Effect on the Enantioselectivity

Narasaka, Koichi,Inoue, Masayuki,Yamada, Tohru,Sugimori, Jun,Iwasawa, Nobuharu

, p. 2409 - 2412 (2007/10/02)

A remarkable effect of solvent on the enantioselectivity was observed in the asymmetric Diels-Alder reaction of 3-(2-alkenoyl)-1,3-oxazolidin-2-ones and dienes catalyzed by a chiral titanium reagent, and the Diels-Alder adducts were obtained in high enant

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