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108351-04-8

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108351-04-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108351-04-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,5 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108351-04:
(8*1)+(7*0)+(6*8)+(5*3)+(4*5)+(3*1)+(2*0)+(1*4)=98
98 % 10 = 8
So 108351-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H8N2O2/c4-2-1-3-5(6)7/h1-4H2

108351-04-8SDS

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 3-nitropropan-1-amine

1.2 Other means of identification

Product number -
Other names 3-Nitro-1-propylamine

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:108351-04-8 SDS

108351-04-8Downstream Products

108351-04-8Relevant articles and documents

Oxidation of azides by the HOF·CH3CN: A novel synthesis of nitro compounds

Carmeli, Mira,Rozen, Shlomo

, p. 4585 - 4589 (2007/10/03)

The HOF·CH3CN complex, readily prepared by passing F 2 through aqueous acetonitrile, is an exceptionally efficient oxygen transfer agent. It is unique in its capacity to oxidize various azides into the corresponding nitro derivatives. This method requires short reactions times and room temperature or below, and the desired nitro compounds were usually isolated in very good yields. The respective nitroso derivatives are believed to be the intermediates in this reaction. Functional groups such as aromatic rings, ketones, nitriles, halides, alcohols, and esters are tolerated. Sulfides react with HOF·CH3CN usually at the same rate as azides. Amines and olefins, however, react faster, so they have to be protected first. Nitro derivatives with various oxygen isotopes can be made using the labeled H 18OF·CH3CN. In the case of chiral azides the stereochemistry around the nitrogen-bonded carbons is retained.

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