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782482-50-2

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782482-50-2 Usage

General Description

(S)-2-(tert-butylamino)-1-(2,4-difluorophenyl)ethanol is a chemical compound with the molecular formula C14H21F2NO. It is a tertiary amine that contains a hydroxyl group and a fluoro-substituted aromatic ring. (S)-2-(TERT-BUTYLAMINO)-1-(2,4-DIFLUOROPHENYL)ETHANOL is used as a chiral building block in the synthesis of pharmaceuticals and other biologically active molecules. Its properties make it suitable for use in asymmetric synthesis and as a chiral auxiliary in organic reactions. (S)-2-(tert-butylamino)-1-(2,4-difluorophenyl)ethanol is an important intermediate in the production of various drugs and can be used to create enantiomerically pure compounds with specific pharmacological properties. (S)-2-(TERT-BUTYLAMINO)-1-(2,4-DIFLUOROPHENYL)ETHANOL has potential applications in the pharmaceutical and agrochemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 782482-50-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,2,4,8 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 782482-50:
(8*7)+(7*8)+(6*2)+(5*4)+(4*8)+(3*2)+(2*5)+(1*0)=192
192 % 10 = 2
So 782482-50-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H17F2NO/c1-12(2,3)15-7-11(16)9-5-4-8(13)6-10(9)14/h4-6,11,15-16H,7H2,1-3H3/t11-/m1/s1

782482-50-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S)-2-(tert-butylamino)-1-(2,4-difluorophenyl)ethanol

1.2 Other means of identification

Product number -
Other names (S)-2-(tert-Butylamino)-1-(2,4-difluorophenyl)ethanol

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:782482-50-2 SDS

782482-50-2Relevant articles and documents

ACYLATED PIPERIDINE DERIVATIVES AS MELANOCORTIN-4 RECEPTOR AGONISTS

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Page/Page column 52-53, (2008/06/13)

Certain novel N-acylated piperidine derivatives are agonists of the human melanocortin receptor(s) and, in particular, are selective agonists of the human melanocortin-4 receptor (MC-4R). They are therefore useful for the treatment, control, or prevention

Enantioselective nitrile anion cyclization to substituted pyrrolidines. A highly efficient synthesis of (3S,4R)-N-tert-butyl-4-arylpyrrolidine-3- carboxylic acid

Chung, John Y. L.,Cvetovich, Raymond,Amato, Joseph,McWilliams, J. Christopher,Reamer, Robert,DiMichele, Lisa

, p. 3592 - 3601 (2007/10/03)

(Chemical Equation Presented) A practical asymmetric synthesis of N-tert-butyl disubstituted pyrrolidines via a nitrile anion cyclization strategy is described. The five-step chromatography-free synthesis of (3S,4R)-1-tert-butyl-4-(2,4-difluorophenyl)pyrr

BICYCLIC PIPERIDINE DERIVATIVES AS MELANOCORTIN-4 RECEPTOR AGONISTS

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Page/Page column 58, (2010/02/08)

Certain novel bicyclic N-acylated piperidine derivatives are agonists of the human melanocortin receptor(s) and, in particular, are selective agonists of the human melanocortin-4 receptor (MC-4R). They are therefore useful for the treatment, control, or p

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