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2684-60-8

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2684-60-8 Usage

General Description

2-Diazopropane, also known as diazopropane or DAP, is a chemical compound with the molecular formula C3H6N2. It is a colorless gas at room temperature and is highly flammable. 2-Diazopropane is primarily used in organic synthesis as a diazo compound, which allows for the introduction of a diazo group into organic molecules. It is also used as a reagent in the preparation of various compounds, including dyes, pharmaceuticals, and other organic chemicals. Additionally, 2-diazopropane can undergo a variety of chemical reactions, including decomposition under heat or light to form nitrogen gas and a carbene intermediate, which can then react with other molecules to form new carbon-carbon bonds. Due to its potentially hazardous nature, proper safety precautions should be taken when handling and using 2-diazopropane.

Check Digit Verification of cas no

The CAS Registry Mumber 2684-60-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,8 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2684-60:
(6*2)+(5*6)+(4*8)+(3*4)+(2*6)+(1*0)=98
98 % 10 = 8
So 2684-60-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H6N2/c1-3(2)5-4/h1-2H3

2684-60-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Diazopropane

1.2 Other means of identification

Product number -
Other names diazo-2-propane

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:2684-60-8 SDS

2684-60-8Relevant articles and documents

UV-laser photochemistry: Retro-cleavage in the benzophenone-sensitized photolysis of Δ3-1,3,4-oxadiazolines into diazoalkanes

Adam, Waldemar,Finzel, Ralf

, p. 863 - 866 (2007/10/02)

Triplet-sensitized photolysis of 2-methoxy-2,5,5-trimethyl-Δ3-1,3,4-oxadiazoline (1a) led to the retro-cleavage products diazoalkane 2a and the ester 3a, for which the triplet diazenyl diradical 6a is postulated as precursor.

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