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10224-14-3

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10224-14-3 Usage

Abbreviation

DPCN

Physical appearance

White to off-white crystalline powder

Solubility

Insoluble in water, soluble in organic solvents

Primary use

Building block in organic synthesis

Application areas

Production of pharmaceuticals and agricultural chemicals

Additional use

Reagent in the preparation of various organic compounds

Hazardous nature

Potentially hazardous chemical

Safety precautions

Handle with caution to avoid skin, eye, and respiratory system irritation

Check Digit Verification of cas no

The CAS Registry Mumber 10224-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,2 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10224-14:
(7*1)+(6*0)+(5*2)+(4*2)+(3*4)+(2*1)+(1*4)=43
43 % 10 = 3
So 10224-14-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H13N/c17-12-16(14-9-5-2-6-10-14)11-15(16)13-7-3-1-4-8-13/h1-10,15H,11H2

10224-14-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-diphenylcyclopropane-1-carbonitrile

1.2 Other means of identification

Product number -
Other names 1,2-diphenylcyclopropanecarbonitrile

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:10224-14-3 SDS

10224-14-3Downstream Products

10224-14-3Relevant articles and documents

Reactions of hypervalent iodonium alkynyl triflates with azides: Generation of cyanocarbenes

Hyatt, I. F. Dempsey,Croatt, Mitchell P.

, p. 7511 - 7514 (2012/09/21)

HIAT me, baby, one more time: Cyanocarbenes have been formed by the reaction of azides with hypervalent iodonium alkynyl triflates (HIATs). Experimental evidence supports the potential intermediacy of an azide-substituted vinylidene or alkynyl azide, both of which could form a cyanocarbene. Trapping of the vinylidene and cyanocarbene includes O-H insertion, dimethyl sulfoxide coordination, and cyclopropanation reactions. Copyright

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