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88721-85-1

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88721-85-1 Usage

Molecular Weight

139.24 g/mol

Structure

Bicyclic with a nitrogen atom

Functional Group

Amine (-NH2)

Appearance

Colorless to pale yellow liquid or solid

Solubility

Soluble in water, ethanol, and other polar solvents

Boiling Point

234-236°C

Melting Point

54-56°C

Density

0.95 g/cm3

Reactivity

Reacts with acids to form salts, and with alkyl halides in nucleophilic substitution reactions

Uses

Building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals

Applications

Modifying the activity and selectivity of drugs and other bioactive molecules

Importance

Versatile intermediate in chemical reactions, valuable compound in the field of organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 88721-85-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,2 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88721-85:
(7*8)+(6*8)+(5*7)+(4*2)+(3*1)+(2*8)+(1*5)=171
171 % 10 = 1
So 88721-85-1 is a valid CAS Registry Number.

88721-85-1SDS

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 1-azabicyclo[3.3.1]nonan-4-amine

1.2 Other means of identification

Product number -
Other names (RS)-endo-4-amino-1-azabicyclo[3.3.1]nonane

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:88721-85-1 SDS

88721-85-1Upstream product

88721-85-1Relevant articles and documents

SYNTHESIS

-

Page/Page column 29-30; 38, (2010/02/11)

The present invention relates to an improved process for the production of [(±)-endo]-4-amino-5-chloro-2-methoxy-N-(I-azabicyclo[3.3. 1]non-4-yl)benzamide hydrochloride, and intermediates thereof.

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