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25635-22-7

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25635-22-7 Usage

General Description

RARECHEM AL BI 0482 is the chemical compound with the Chemical Abstracts Service (CAS) number 847955-32-3. It is also known by its other names like (R)-tert-butyl N-((1R,2S)-2-(methylamino)cyclohexyl)carbamate and (R)-t-Butyl-(1R,2S)-methylcarbamoylcyclohexylamine. It has a molecular formula of C11H23N2O2 and a molecular weight of 213.31 g/mol. RARECHEM AL BI 0482 is used in chemical research and pharmaceutical development, and it may have potential applications in the synthesis of pharmaceutical drugs or as a building block in organic synthesis. It is important to handle and use this chemical with caution, following proper safety protocols and guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 25635-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,6,3 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25635-22:
(7*2)+(6*5)+(5*6)+(4*3)+(3*5)+(2*2)+(1*2)=107
107 % 10 = 7
So 25635-22-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO2/c1-2-15-12(14)10-7-3-5-9-6-4-8-13-11(9)10/h3-8H,2H2,1H3

25635-22-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl quinoline-8-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 8-quinolinecarboxylate

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:25635-22-7 SDS

25635-22-7Relevant articles and documents

-

Smolentseva et al.

, (1975)

-

Chiral 1,2,3,4-tetrahydroquinolinyl-oxazoline ligands for Ru-catalyzed asymmetric transfer hydrogenation of ketones

Zhou, Yi-Bo,Tang, Fang-Yi,Xu, Hua-Dong,Wu, Xin-Yan,Ma, Jun-An,Zhou, Qi-Lin

, p. 469 - 473 (2007/10/03)

Chiral 1,2,3,4-tetrahydroquinolinyl-oxazoline compounds have been synthesized from 8-quinolinecarboxylic acid and enantiomerically pure amino alcohols using a convenient procedure. Asymmetric transfer hydrogenation of aryl ketones with the catalyst prepared in situ from [Ru(p-cymene)Cl2]2 and ligands 2 in 2-propanol in the presence of KOH, afforded the corresponding secondary alcohols in reasonable yields and up to 83% e.e.

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