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2-aminocyclooctanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1551-75-3

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1551-75-3 Usage

Appearance

White to off-white crystalline

Solubility

Soluble in water and organic solvents

Functional Groups

Primary amine group

Uses

Chiral resolving agent, building block in pharmaceuticals and agricultural chemicals

Potential applications

Asymmetric catalysis, medicinal chemistry

Potential activities

Anti-cancer, anti-inflammatory

Check Digit Verification of cas no

The CAS Registry Mumber 1551-75-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,5 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1551-75:
(6*1)+(5*5)+(4*5)+(3*1)+(2*7)+(1*5)=73
73 % 10 = 3
So 1551-75-3 is a valid CAS Registry Number.

1551-75-3SDS

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 2-aminocyclooctan-1-ol

1.2 Other means of identification

Product number -
Other names 2-aminocyclooctanol

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:1551-75-3 SDS

1551-75-3Relevant academic research and scientific papers

Asymmetric Catalysis by Vitamin B12: The Isomerization of Achiral Aziridines to Optically Active Allylic Amines

Zhang, Zhong da,Scheffold, Rolf

, p. 2602 - 2615 (2007/10/02)

Achiral N-acylaziridines are isomerized to optically active N-acyl-allylamines in ee's of up to 95percent by catalytic amounts of cob(I)alamin in MeOH.

The Reaction between trans-2-Alkylaminocycloalkanols and Formaldehyde

Barkworth, Peter M. R.,Crabb, Trevor A.

, p. 260 - 264 (2007/10/02)

trans-2-Alkylaminocyclohexanols and trans-2-alkylaminocycloheptanols condense with formaldehyde to give perhydrocycloalkanooxazoles, whereas trans-2-alkylaminocyclopentanols give rise to perhydrocyclopentanodioxazepines.The two types of ring systems are characterized by differing proton-proton geminal coupling constants and 13C NMR parameters.

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