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14763-63-4

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14763-63-4 Usage

General Description

Phenol, 4-(phenylsulfinyl)- is a chemical compound that belongs to the class of phenols, which are organic compounds that contain a hydroxyl group attached to an aromatic ring. The 4-(phenylsulfinyl) group indicates the presence of a phenyl ring attached to a sulfur atom with a double bond to an oxygen atom. Phenol, 4-(phenylsulfinyl)- may have various industrial and research applications, including in the production of pharmaceuticals, pesticides, and organic synthesis. Additionally, it may also have potential biological activities, making it of interest for further study in the fields of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 14763-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,6 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14763-63:
(7*1)+(6*4)+(5*7)+(4*6)+(3*3)+(2*6)+(1*3)=114
114 % 10 = 4
So 14763-63-4 is a valid CAS Registry Number.

14763-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(benzenesulfinyl)phenol

1.2 Other means of identification

Product number -
Other names p-Hydroxyphenyl-phenyl-sulfoxid

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:14763-63-4 SDS

14763-63-4Downstream Products

14763-63-4Relevant articles and documents

Methyl sulfinates as electrophiles in friedel-crafts reactions. Synthesis of aryl sulfoxides

Yuste, Francisco,Hernandez Linares, Angelica,Mastranzo, Virginia M.,Ortiz, Benjamin,Sanchez-Obregon, Ruben,Fraile, Alberto,Garcia Ruano, Jose Luis

, p. 4635 - 4644 (2011/07/29)

The Friedel-Crafts reaction of methyl alkyl- and arylsulfinates with aromatic systems, activated by one or more electron-donating substituents (OH, OMe, NHR, NR2), provides alkyl aryl and diaryl sulfoxides under mild conditions and in moderate to good yields. The very high regioselectivity usually observed in these sulfinylation reactions is rationalized on the basis of a Wheland intermediate having a trigonal bypyramidal structure in which steric and electronic interactions are significant factors strongly destabilizing the attack to the ortho positions.

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