Welcome to LookChem.com Sign In|Join Free

CAS

  • or

13374-31-7

Post Buying Request

13374-31-7 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

13374-31-7 Usage

Chemical Properties

White crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 13374-31-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,7 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13374-31:
(7*1)+(6*3)+(5*3)+(4*7)+(3*4)+(2*3)+(1*1)=87
87 % 10 = 7
So 13374-31-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO.ClH/c7-5-3-1-2-4-6(5)8;/h5-6,8H,1-4,7H2;1H/t5-,6-;/m1./s1

13374-31-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (671762)  (1R,2R)-trans-2-Aminocyclohexanolhydrochloride  95.0-105.0% (AT)

  • 13374-31-7

  • 671762-250MG

  • 637.65CNY

  • Detail
  • Aldrich

  • (671762)  (1R,2R)-trans-2-Aminocyclohexanolhydrochloride  95.0-105.0% (AT)

  • 13374-31-7

  • 671762-1G

  • 2,129.40CNY

  • Detail

13374-31-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2R)-Trans-2-AminoCyclohexanol Hydrochloride

1.2 Other means of identification

Product number -
Other names (1R,2R)-2-Aminocyclohexanol hydrochloride

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:13374-31-7 SDS

13374-31-7Relevant articles and documents

An efficient and highly selective cleavage of N-tert- butoxycarbonyl group under microwave irradiation

Bose, D. Subhas,Lakshmiriarayana

, p. 5631 - 5634 (1998)

A simple and high yielding method for the cleavage of t-Boc carbamates is described which occurs under mild and solvent-free conditions using microwave irradiation.

6-O-SUBSTITUTED BENZOXAZOLE AND BENZOTHIAZOLE COMPOUNDS AND METHODS OF INHIBITING CSF-1R SIGNALING

-

Page/Page column 101, (2008/06/13)

Benzoxazole and benzothiazole compounds and the stereoisomers, tautomers, solvates, oxides, esters, and prodrugs thereof and pharmaceutically acceptable salts thereof are disclosed. Compositions of the compounds, either alone or in combination with at least one additional therapeutic agent, with a pharmaceutically acceptable carrier, and uses of the compounds, either alone or in combination with at least one additional therapeutic agent are also disclosed. The embodiments are useful for inhibiting cellular proliferation, inhibiting the growth and/or metathesis of tumors, treating or preventing cancer, treating or preventing degenerating bone diseases such as rheumatoid arthritis, and/or inhibiting molecules such as CSF-1R.

Stereocontrolled Preparation of Cyclohexane Amino Alcohols Utilising a Modified Mitsunobu Reaction

Sammes, Peter G.,Thetford, Dean

, p. 655 - 661 (2007/10/02)

A method for the introduction of amino groups into aliphatic systems is described.Cyclohex-2-enol reacts with aromatic diacylamines under Mitsunobu reaction conditions to give either N-alkylated or O-alkylated products in a controlled, predictable manner.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 13374-31-7