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1-Cyclopentene-1-carboxylic acid, 2-[[(1R)-1-phenylethyl]amino]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

683774-02-9

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683774-02-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 683774-02-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,3,7,7 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 683774-02:
(8*6)+(7*8)+(6*3)+(5*7)+(4*7)+(3*4)+(2*0)+(1*2)=199
199 % 10 = 9
So 683774-02-9 is a valid CAS Registry Number.

683774-02-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-{[(R)-1-phenylethyl]amino}cyclopent-1-ene-1-carboxylate

1.2 Other means of identification

Product number -
Other names methyl (1'R) 2-[(1-phenylethyl)amino]-1-cyclopentene-1-carboxylate

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:683774-02-9 SDS

683774-02-9Relevant academic research and scientific papers

Synthesis, preliminary biological evaluation and molecular modeling of some new heterocyclic inhibitors of TACE

Sengupta, Prabal,Puri, Chetan S.,Chokshi, Hemant A.,Sheth, Chetana K.,Midha, Ajay S.,Chitturi, Trinadha Rao,Thennati, Rajamannar,Murumkar, Prashant R.,Yadav, Mange Ram

, p. 5549 - 5555 (2011/12/15)

Central heteroaryl ring analogues belonging to a series of potent hydroxamate TACE inhibitors were synthesized. The TACE inhibitory activities of these compounds were evaluated by in vitro WBA and in silico molecular modeling studies using crystal structure of human TACE. Compound 14 showed very good in vitro inhibition, supported by the in silico docking studies.

Total Synthesis of (-)-13-acetoxymodhephene and (+)-14-acetoxymodhephene

Lee, Hee-Yoon,Murugan, Ravichandran N.,Moon, Deuk Kyu

experimental part, p. 5028 - 5037 (2010/02/28)

Stereoselective epoxidation of [4.3.3]propellane 16 set the stage for the Lewis acid catalyzed stereospecific ring contraction to an oxygenated modhephene structure and eventually led to the total synthesis of (-)-13-acetoxymodhephene and (+)- 14-acetoxym

Enantioselective synthesis of (R)-1-azaspiro-[4.4]nonane-2,6-dione ethylene ketal, key chiral intermediate in the elaboration of (-)-cephalotaxine

Pizzonero, Mathieu,Dumas, Francoise,d'Angelo, Jean

, p. 31 - 37 (2007/10/03)

An enantioselective synthesis of (R)-1-azaspiro[4.4]nonane-2,6-dione ethylene ketal (4), chiral relay in the elaboration of (-)-cephalotaxine (1b), starting from (R)-1-(2-methoxycarbonylethyl)-2-oxo-cyclopentanecarboxylic acid methyl ester ((R)-10) (8 chemical operations, 26% overall yield, ee ≥ 95%) is described. The Curtius rearrangement of acyl azide (12) was used as the key strategic element to install with a perfect stereochemical fidelity and a high efficiency an α-nitrogen substituent at the quaternary carbon center in 10.

The asymmetric Michael-type alkylation of chiral β-enamino esters: Critical role of a benzyl ester group in the racemization of adducts

Pizzonero, Mathieu,Hendra, Frederic,Delarue-Cochin, Sandrine,Tran Huu-Dau, Marie-Elise,Dumas, Francoise,Cave, Christian,Nour, Mohammed,D'Angelo, Jean

, p. 3853 - 3857 (2007/10/03)

In contrast with keto diester (R)-10a bearing a methyl ester group at the quaternary carbon center, the benzyl ester analogue (R)-10a partially racemized during workup, thereby revealing that the nature of the ester group at the quaternary carbon center h

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