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Cyclopropane amine, also known as aziridine, is a cyclic amine with the chemical formula C3H7N. It is a colorless, highly reactive, and toxic liquid with a pungent odor. Cyclopropane amine is a member of the aziridine family, which are cyclic amines with a three-membered nitrogen-containing ring. Due to its high reactivity, it is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its ability to react with electrophilic reagents and undergo ring-opening reactions, making it a valuable building block in organic chemistry. However, due to its toxicity and potential to cause severe health issues, it requires careful handling and storage.

965-30-0

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965-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 965-30-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 965-30:
(5*9)+(4*6)+(3*5)+(2*3)+(1*0)=90
90 % 10 = 0
So 965-30-0 is a valid CAS Registry Number.

965-30-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name azane,cyclopropane

1.2 Other means of identification

Product number -
Other names benzaldehyde O-(p-nitrobenzoyl)oxime

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:965-30-0 SDS

965-30-0Downstream Products

965-30-0Relevant academic research and scientific papers

The Photochemistry of α-Nitrostilbenes and Related Compounds. A Study of Double Bond Cleavage Following Intramolecular Cyclization and Nitro-Nitrite Rearrangement

Grant, Richard D.,Pinhey, John T.,Rizzardo, Ezio

, p. 1217 - 1229 (2007/10/02)

A detailed study of the photochemistry of a number of α-nitrostilbenes is reported.The previously described intramolecular cyclization of (1) which resulted in cleavage of the double bond was not found to occur to any extent in the other compounds examined.The majority of the compounds were found to yield significant amounts of aldehydes and nitriles, which result from a new fragmentation pathway arising from initial photochemical nitro-nitrite isomerization.

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