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71581-92-5

71581-92-5

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71581-92-5 Usage

Chemical Properties

white to light yellow crystal powde

Check Digit Verification of cas no

The CAS Registry Mumber 71581-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,8 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71581-92:
(7*7)+(6*1)+(5*5)+(4*8)+(3*1)+(2*9)+(1*2)=135
135 % 10 = 5
So 71581-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H21NO/c16-11-13-8-4-5-9-14(13)15-10-12-6-2-1-3-7-12/h1-3,6-7,13-16H,4-5,8-11H2/p+1/t13-,14-/m0/s1

71581-92-5 Well-known Company Product Price

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  • TCI America

  • (B1119)  (+)-cis-2-Benzylaminocyclohexanemethanol  >98.0%(T)

  • 71581-92-5

  • 1g

  • 1,350.00CNY

  • Detail

  • TCI America

  • (B1119)  (+)-cis-2-Benzylaminocyclohexanemethanol  >98.0%(T)

  • 71581-92-5

  • 5g

  • 4,990.00CNY

  • Detail

  • Alfa Aesar

  • (L09603)  cis-(1R,2S)-(+)-2-Benzylaminocyclohexanemethanol, 98%   

  • 71581-92-5

  • 250mg

  • 176.0CNY

  • Detail

  • Alfa Aesar

  • (L09603)  cis-(1R,2S)-(+)-2-Benzylaminocyclohexanemethanol, 98%   

  • 71581-92-5

  • 1g

  • 615.0CNY

  • Detail

71581-92-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2S)-(+)-cis-2-(Benzylamino)cyclohexanemethanol

1.2 Other means of identification

Product number -
Other names (+)-CIS-2-BENZYLAMINOCYCLOHEXANEMETHANOL

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:71581-92-5 SDS

71581-92-5Relevant articles and documents

Chirality control by substituents in the asymmetric addition of Et2Zn to aromatic aldehydes catalyzed by cis-(1R,2S)-2-benzamidocyclohexanecarboxylic acid derived 1,3-aminoalcohols

Wang, Xiangbo,Kodama, Koichi,Hirose, Takuji,Zhang, Guangyou

experimental part, p. 61 - 68 (2010/09/05)

A series of novel optically active 1,3-aminoalcohols based on cis-(1R,2S)-2-benzamidocyclohexanecarboxylic acid and trans-(1R,2R)-2-benzamidocyclohexanecarboxylic acid were synthesized and used in the asymmetric diethylzinc addition to aromatic aldehydes.

A CONVENIENT SYNTHESIS OF cis-(1R)-N-BENZYL-(2S)-(HYDROXYMETHYL)CYCLOHEXYLAMINE

Vanderplas, B.,Murtiashaw, C. W.,Sinay, T.,Urban, F. J.

, p. 685 - 687 (2007/10/03)

-

STEREOCHEMICAL STUDIES-76 SATURATED HETEROCYCLES-63 SYNTHESIS OF CIS- AND TRANS-N-METHYL- AND N-BENZYL-4,5- AND 5,6-TETRAMETHYLENETETRAHYDRO-1,3-OXAZINES; AN X-RAY STUDY OF N-BENZYL-CIS-4,5-TETRAMETHYLENETETRAHYDRO-1,3-OXAZINIUM-PICRATE

Fulop, Ferenc,Bernath, Gabor,Argay, Gyula,Kalman, Alajos,Sohar, Pal

, p. 2053 - 2060 (2007/10/02)

The corresponding cis- and trans-N-methyl- and N-benzyl-5,6- and 4,5-tetramethylenetetrahydro-1,3-oxazines (5a,b-8a,b) were synthesized from cis- and trans-N-methyl- and N-benzyl-2-aminomethyl-1-cyclohexanols (1a,b,2 2a,b), and from cis- and trans-N-methy

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