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p-tert-Butyl-thiophenol is a chemical compound with the molecular formula C10H14S, belonging to the class of thiophenols. It features a thiophene ring with a thiol group attached and is distinguished by the presence of a tert-butyl group, a branched alkyl group. Known for its strong, distinct odor, p-tert-Butyl-thiophenol is utilized in various applications due to its unique chemical properties.

4946-15-0

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4946-15-0 Usage

Uses

Used in Fragrance and Flavor Industry:
p-tert-Butyl-thiophenol is used as a fragrance and flavor ingredient for its strong, distinct scent. It is incorporated into personal care items and food products, typically in small quantities, to impart a characteristic aroma to the final product.
Used in Organic Synthesis:
p-tert-Butyl-thiophenol serves as a valuable intermediate in organic synthesis, contributing to the creation of various complex organic compounds.
Used in Pharmaceutical Production:
p-tert-Butyl-thiophenol has potential applications in the pharmaceutical industry, where it may be utilized in the development and production of new drugs.
Used in Agrochemicals:
p-tert-Butyl-thiophenol also finds use in the agrochemical sector, potentially playing a role in the synthesis of pesticides or other agricultural chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 4946-15-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,4 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4946-15:
(6*4)+(5*9)+(4*4)+(3*6)+(2*1)+(1*5)=110
110 % 10 = 0
So 4946-15-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H14S/c1-2-3-4-9-5-7-10(11)8-6-9/h5-8,11H,2-4H2,1H3

4946-15-0SDS

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 4-Butylbenzenethiol

1.2 Other means of identification

Product number -
Other names 4-butylthiophenol

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:4946-15-0 SDS

4946-15-0Relevant articles and documents

Potent and Specific Inhibition of NTCP-Mediated HBV/HDV Infection and Substrate Transporting by a Novel, Oral-Available Cyclosporine A Analogue

Liu, Yang,Ruan, Hanying,Li, Ying,Sun, Guoliang,Liu, Xiao,He, Wenhui,Mao, Fengfeng,He, Miaomiao,Yan, Liwei,Zhong, Guocai,Yan, Huan,Li, Wenhui,Zhang, Zhiyuan

supporting information, p. 543 - 565 (2021/01/13)

Analogues of the natural product cyclosporine A (CsA) were developed and assessed as antivirals against infection of hepatitis B virus (HBV) and its satellite hepatitis D virus (HDV). An analogue termed 27A exhibits potent inhibition of HBV/HDV infection by specifically blocking viral engagement to its cellular receptor NTCP, while it lacks immunosuppressive activity found in natural CsA. Intraperitoneal injection or oral intake of 27A protects HDV-susceptible mouse model from HDV infection. 27A serves as a promising lead for the development of novel anti-HDV/HBV agents.

NTCP INHIBITORS

-

Paragraph 0136, (2019/11/04)

Provided are cyclosporin A analogues that are NTCP inhibitors and useful for treating HBV and/or HDV infection (s), hepatoprotection and amelioration of hypercholesterolemia, diabetes and inhibiting cancer.

Theoretical and Spectroscopical Investigations of Indigo Dyes, XXII. - Preparations of 5,5'- and 6,6'-Dialkylated Indigo Dyes

Meier, Helmut,Luettke, Wolfgang

, p. 1303 - 1333 (2007/10/02)

The manifolded applicabilities of indigo dyes are strongly restricted by the low solubility of most of their representatives.We describe in this paper the preparation of a series of dialkylated indigos 1, thioindigos 2, dyes of the cibaviolett-type 3, and of the corresponding vinylogues 4, 5, and 6 by different synthetic methods.Some of the prepared compounds show a remarkable solubility and can be used for spectroscopic measurements even in non-polar solvents.

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