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1-(prop-2-en-1-ylsulfanyl)naphthalene, also known as allylthionaphthalene, is a chemical compound with the molecular formula C14H12S. It is a yellow solid with a naphthalene-like odor.
Used in Fragrance Industry:
1-(prop-2-en-1-ylsulfanyl)naphthalene is used as a fragrance ingredient for its naphthalene-like odor.
Used in Pharmaceutical Industry:
1-(prop-2-en-1-ylsulfanyl)naphthalene is used as a potential candidate for pharmaceutical products due to its antimicrobial and antioxidant properties.
Used in Cosmetic Industry:
1-(prop-2-en-1-ylsulfanyl)naphthalene is used as a potential candidate for cosmetic products due to its antimicrobial and antioxidant properties.

51621-72-8

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51621-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51621-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,2 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51621-72:
(7*5)+(6*1)+(5*6)+(4*2)+(3*1)+(2*7)+(1*2)=98
98 % 10 = 8
So 51621-72-8 is a valid CAS Registry Number.

51621-72-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-prop-2-enylsulfanylnaphthalene

1.2 Other means of identification

Product number -
Other names -

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:51621-72-8 SDS

51621-72-8Relevant academic research and scientific papers

ALLOSTERIC BINDING COMPOUNDS

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Page/Page column 22, (2012/04/23)

The present invention relates to allosteric binding compounds of formula (I), especially for the treatment of CNS disorders, together with pharmaceutical compositions and methods of treatment including these compounds.

POTASSIUM TRIISOPROPYLSILANETHIOLATE: VINYL AND ARYL SULFIDES THROUGH Pd-CATALYZED CROSS COUPLING

Rane, Anil M.,Miranda, Edgar I.,Soderquist, John A.

, p. 3225 - 3226 (2007/10/02)

Vinyl and aryl halides are efficiently converted, under Pd catalysis, with KSTIPS (1) to the corresponding silyl sulfides (2, 3).The naphthyl derivative was easily hydrolyzed to the mercaptan 4, or alkylated or alkenylated to provide unsymmetrical sulfides (5, 6).

2-ALKENYL ARYL SULFOXIDES IN THE PUMMERER REACTION

Fedorov, N. V.,Anisimov, A. V.,Viktorova, E. A.

, p. 507 - 511 (2007/10/02)

The reaction of 2-alkenyl aryl sulfoxides with the mixed anhydride of acetic and trifluoroacetic acids leads to the corresponding α-acetoxy-substituted sulfides.The action of acetic acid on 2-alkenyl 1-naphthyl sulfoxides leads to the formation of substituted dihydronaphthothiophene 1-oxides.Diaryl disulfides and 2-alkenyl aryl sulfides are formed as side products.

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