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83150-77-0

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83150-77-0 Usage

Description

(S)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methanethiol is a chemical compound that belongs to the thiol class, characterized by the presence of a sulfhydryl group. It is known for its strong and distinct odor, making it a valuable component in various applications.

Uses

Used in Fragrance Industry:
(S)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methanethiol is used as a fragrant component in perfumes and colognes due to its unique and pungent aroma, contributing to the overall scent profile of these products.
Used in Food Industry:
In the food industry, (S)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methanethiol is used as a flavoring agent, responsible for enhancing the characteristic smell and taste of certain food items.
Used in Consumer Products:
(S)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methanethiol is used as a fragrant and flavoring agent in various consumer products, adding to their appeal and sensory experience.
Used in Chemical Synthesis:
(S)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methanethiol serves as an important building block in the synthesis of other chemicals, making it a crucial component in the production process.
Used in Pharmaceutical Production:
It is utilized in the production of pharmaceuticals, where its unique properties contribute to the development of various medicinal compounds.
Used in Dye Manufacturing:
(S)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methanethiol is also used in the manufacturing of dyes, playing a role in the creation of colorants for different applications.
Used in Other Industrial Applications:
(S)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methanethiol finds use in a range of other industrial applications, where its distinctive characteristics are harnessed for specific purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 83150-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,1,5 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83150-77:
(7*8)+(6*3)+(5*1)+(4*5)+(3*0)+(2*7)+(1*7)=120
120 % 10 = 0
So 83150-77-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H18S/c1-8-4-6-9(7-5-8)10(2,3)11/h4,9,11H,5-7H2,1-3H3/t9-/m1/s1

83150-77-0Downstream Products

83150-77-0Relevant articles and documents

Method for preparing 1-poxlene -8-thiol

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Paragraph 0039-0103, (2019/06/27)

The invention belongs to the technical field of fine chemistry, and provides a method for preparing 1-poxlene-8-thiol, wherein a-terpineol is used as a raw material, and the a-terpineol reacts with athioreagent to obtain the 1-poxlene -8-thiol, the method comprises the following steps: dissolving the a-terpineol in an organic solvent; adding the thioreagent in batches to carry out a thioreaction;the system after reaction is cooled to room temperature, the solvent is removed through rotating evaporation, and sodium hydroxide aqueous solution is slowly added until the pH value is more than orequal to 12; extracting the water phase with methyl tert-ether twice, combining the organic phase, washing with saturated brine once, drying with anhydrous sodium sulfate, concentrating, and distilling under reduced pressure to obtain the product 1-poxlene-8-thiol. The method solves the problems that in the prior art, the synthesis route of the 1-poxlene-8-thiol is complex, the lithium aluminum tetrahydrate in the raw material is expensive, the danger is high, and the prior method is not suitable for industrial production.

Synthesis process method of p-menon-1-ene-8-thiol

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Paragraph 0017; 0019; 0020; 0022; 0023; 0025; 0026; 0028, (2019/04/26)

The invention discloses a synthesis process method of p-menon-1-ene-8-thiol, in particular to a novel synthesis process method for obtaining p-menon-1-ene-8-thiol by using cheap synthetic perfume alpha-terpineol obtained from turpentine oil as a raw material to be reacted with thioacetic acid and then adopting LiAlH4 for reduction. The synthesis process method has the advantages that the synthesisroute is short, the process operation is simple, raw materials and reagents are easy to obtain and cheap, the first reaction cycle is shortened, the yield is high, and more importantly, the cost is greatly reduced.

Simple synthetic protocols for tertiary alkyl and allyl thiols

Gurudutt, K. N.,Rao, Sanjay,Srinivas, P.,Srinivas, S.

, p. 1169 - 1171 (2007/10/03)

Convenient preparative methods for tertiary alkyl and allyl thiols are described. Accordingly, thiolesters and thiocyanates, obtained from the reaction of SN1-active halides and appropriate zinc salts, on hydrolysis and LAH reduction respectively, afford the corresponding thiols in near quantitative yields. Besides the well known p-menth-1-ene-8-thiol, p-menthane-1-thiol, p-mentha-1,8-diene-6-thiol and 2-(2-phenyl)propane thiol have been prepared.

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