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6415-70-9

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6415-70-9 Usage

General Description

2,3-diphenylcycloprop-2-ene-1-carboxamide is a chemical compound with the molecular formula C17H13NO. It is an amide derivative of a cyclopropene compound, containing two phenyl groups attached to the cyclopropene ring. 2,3-diphenylcycloprop-2-ene-1-carboxamide is an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is known for its potential as a building block in the development of new drugs and agrochemicals due to its unique structural properties. However, it is important to handle this chemical with care, as it may have potential hazards and health effects if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 6415-70-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6415-70:
(6*6)+(5*4)+(4*1)+(3*5)+(2*7)+(1*0)=89
89 % 10 = 9
So 6415-70-9 is a valid CAS Registry Number.

6415-70-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-diphenylcycloprop-2-ene-1-carboxamide

1.2 Other means of identification

Product number -
Other names 1,2-Diphenyl-cycloprop-1-en-3-carbonsaeure-amid

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:6415-70-9 SDS

6415-70-9Relevant articles and documents

Small Rings, 33. Attempts to Synthesize Diphenyltetrahedrane

White, Emil H.,Winter, Rudolph E. K.,Graeve, Rolf,Zirngibl, Ulrich,Friend, Earl W.,et al.

, p. 3906 - 3915 (2007/10/02)

Carbene 7, formed on photochemical or thermal excitation of (2,3-diphenyl-2-cyclopropen-1-yl)diazomethane (6i), splits mostly into two acetylenes 8 and 9 instead of undergoing an intramolecular cycloaddition.Photolysis of the Masamune ketone 16 depending on the reaction conditions gives either p-terphenyl or a mixture of the two cyclooctatetraens 18 and 19.The intermediate formation of tetrahedrane 10 would fit into the mechanistic picture of this fragmentation.

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