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140836-53-9

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140836-53-9 Usage

Structure

Bicyclic compound with a seven-membered ring containing a nitrogen atom and a hydroxyl group attached to one of the carbon atoms

Uses

Commonly used as a building block in organic synthesis and pharmaceutical research

Pharmaceutical applications

Suitable for the development of central nervous system agents and antipsychotic medications

Therapeutic potential

Valuable for creating a wide range of chemical compounds with therapeutic properties

Check Digit Verification of cas no

The CAS Registry Mumber 140836-53-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,8,3 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 140836-53:
(8*1)+(7*4)+(6*0)+(5*8)+(4*3)+(3*6)+(2*5)+(1*3)=119
119 % 10 = 9
So 140836-53-9 is a valid CAS Registry Number.

140836-53-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-azanorbornene-3-exo-methanol

1.2 Other means of identification

Product number -
Other names (1R,3R,4S)-1-(2-Aza-bicyclo[2.2.1]hept-5-en-3-yl)-methanol

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:140836-53-9 SDS

140836-53-9Downstream Products

140836-53-9Relevant articles and documents

Syntheses and antiulcer activities of 2-aminonorbornene derivatives

Yamazaki,Horikawa,Nishitani,Iwasaki,Nosaka,Tamaki

, p. 102 - 108 (2007/10/02)

2,2,-Disubstituted nothornenes (1, 2), 2,2-Disubstituted nothornane (3), 2,2,3-trisubstituted norbornenes (4, 5), oxanothornenes (6) and azanorbornenes (7) were synthesized by the Diels-Alder reaction using α,β-dehydroamino acids as a key step, and their

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