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2-Cyclobuten-1-one, 3-hydroxy-2,4-diphenyl- is a chemical compound with the molecular formula C16H12O2. It is a derivative of cyclobutenone, featuring a hydroxyl group at the 3-position and two phenyl rings attached to the 2 and 4 positions. This organic compound is known for its unique structure and potential applications in various chemical reactions and synthesis processes. It is an important intermediate in the preparation of certain pharmaceuticals and other organic compounds due to its reactive nature and the presence of both aromatic and cyclic structures.

4683-17-4

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4683-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4683-17-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,8 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4683-17:
(6*4)+(5*6)+(4*8)+(3*3)+(2*1)+(1*7)=104
104 % 10 = 4
So 4683-17-4 is a valid CAS Registry Number.

4683-17-4SDS

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 2,4-diphenyl-3-hydroxycyclobuten-1-one

1.2 Other means of identification

Product number -
Other names 2,4-Diphenyl-3-hydroxy-cyclobutenon

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:4683-17-4 SDS

4683-17-4Relevant academic research and scientific papers

Hydroxylation of carbanions with lithium teri-butyl peroxide acting as an oxenoid

Julia, Marc

, p. 15 - 24 (2007/10/03)

The lithium salt of terf-butyl hydroperoxide can convert alkyl, vinyl, aryl carbanions, acetylides and various enolates into the corresponding hydroxylated derivatives in good yields and under mild conditions. Eisevier.

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