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54576-40-8

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54576-40-8 Usage

General Description

1-Methyl-4-(sec-butylthio)benzene is a chemical compound containing a benzene ring with a methyl group at the 1-position and a sec-butylthio group at the 4-position. 1-Methyl-4-(sec-butylthio)benzene is commonly used in the fragrance industry as a scent ingredient and is known for its aromatic and slightly sweet odor. It is also used as a flavoring agent in food products. In addition to its use in scents and flavors, 1-Methyl-4-(sec-butylthio)benzene is also used in the manufacturing of various industrial products as a chemical intermediate. It is important to handle this compound with caution, as it may be hazardous if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 54576-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,7 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54576-40:
(7*5)+(6*4)+(5*5)+(4*7)+(3*6)+(2*4)+(1*0)=138
138 % 10 = 8
So 54576-40-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H16S/c1-4-10(3)12-11-7-5-9(2)6-8-11/h5-8,10H,4H2,1-3H3

54576-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-butan-2-ylsulfanyl-4-methylbenzene

1.2 Other means of identification

Product number -
Other names sec-Butyl-p-tolyl-sulfid

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:54576-40-8 SDS

54576-40-8Downstream Products

54576-40-8Relevant articles and documents

Reductive α-substitution of sulfoxides with grignard reagents promoted by a magnesium amide

Kobayashi, Kazuhiro,Yokota, Kouichi,Akamatsu, Hideki,Morikawa, Osamu,Konishi, Hisatoshi

, p. 441 - 443 (2007/10/03)

The reactions of sulfoxides bearing α-hydrogen(s) (RSOCHR1R2: R-alkyl or aryl; R1, R2 = H, alkyl, or aryl) with Grignard reagents (R3MgBr: R3 = Et, Ph, or vinyl) in the presence of the diisopropylaminomagnesium reagent, generated in situ by the treatment of diisopropylamine with the appropriate Grignard reagents in diethyl ether, have resulted in the formation of the corresponding sulfides (RSCR1R2R3) in moderate to good isolated yields.

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