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51600-24-9

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51600-24-9 Usage

General Description

(S)-(-)-1-(1-Naphthyl)ethylamine hydrochloride, also known as (S)-(-)-α-methyl-1-naphthalenemethylamine, is a chemical compound with the formula C12H13N. It is a chiral amine that is commonly used in organic synthesis as a building block for various pharmaceuticals and agrochemicals. (S)-(-)-1-(1-NAPHTHYL)ETHYLAMINE HYDROC& is a white to off-white crystalline powder that is soluble in water and ethanol. It is also known for its potential as a ligand in asymmetric catalysis, making it a valuable tool in chemical research and development. Additionally, it is used as a reagent in the synthesis of various biologically active compounds and as a precursor in the production of a wide range of chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 51600-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,0 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51600-24:
(7*5)+(6*1)+(5*6)+(4*0)+(3*0)+(2*2)+(1*4)=79
79 % 10 = 9
So 51600-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H13N.ClH/c1-9(13)11-8-4-6-10-5-2-3-7-12(10)11;/h2-9H,13H2,1H3;1H/t9-;/m0./s1

51600-24-9 Well-known Company Product Price

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  • Aldrich

  • (656747)  (S)-(−)-1-(1-Naphthyl)ethylaminehydrochloride  97%

  • 51600-24-9

  • 656747-1G

  • 621.27CNY

  • Detail
  • Aldrich

  • (656747)  (S)-(−)-1-(1-Naphthyl)ethylaminehydrochloride  97%

  • 51600-24-9

  • 656747-5G

  • 2,129.40CNY

  • Detail

51600-24-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-(-)-1-(1-NAPHTHYL)ETHYLAMINE HYDROC&

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:51600-24-9 SDS

51600-24-9Upstream product

51600-24-9Downstream Products

51600-24-9Relevant articles and documents

Rhodium-catalyzed asymmetric hydrogenation of unprotected NH imines assisted by a thiourea

Zhao, Qingyang,Wen, Jialin,Tan, Renchang,Huang, Kexuan,Metola, Pedro,Wang, Rui,Anslyn, Eric V.,Zhang, Xumu

supporting information, p. 8467 - 8470 (2014/08/18)

Asymmetric hydrogenation of unprotected NH imines catalyzed by rhodium/bis(phosphine)-thiourea provided chiral amines with up to 97% yield and 95% ee. 1HNMR studies, coupled with control experiments, implied that catalytic chloride-bound intermediates were involved in the mechanism through a dual hydrogen-bonding interaction. Deuteration experiments proved that the hydrogenation proceeded through a pathway consistent with an imine.

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