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38185-19-2

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38185-19-2 Usage

Description

4-(METHYLTHIO)BENZYL BROMIDE 97, also known as 4-(methylthio)benzyl bromide, is an organic compound with the chemical formula C7H7BrS. It is a colorless to pale yellow liquid with a distinctive odor. 4-(METHYLTHIO)BENZYL BROMIDE 97 is characterized by the presence of a benzene ring, a methylthio group, and a bromine atom, which contribute to its unique chemical properties and potential applications.

Uses

Used in Chemical Synthesis:
4-(METHYLTHIO)BENZYL BROMIDE 97 is used as a chemical intermediate for the synthesis of various organic compounds. Its reactivity with different functional groups makes it a versatile building block in the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(METHYLTHIO)BENZYL BROMIDE 97 is used as a key intermediate in the synthesis of drugs with potential therapeutic applications. Its unique structure allows for the formation of new chemical entities that can target specific biological pathways, leading to the development of novel treatments for various diseases.
Used in Synthesis of Sulfoxides:
4-(METHYLTHIO)BENZYL BROMIDE 97 is used as a precursor for the synthesis of sulfoxides, which are important compounds in the field of organic chemistry. The self-catalyzed oxidation of this compound in the presence of hydrogen peroxide leads to the formation of the corresponding sulfoxide, which can be further utilized in the synthesis of various organic compounds and materials.
Used in Material Science:
In the field of material science, 4-(METHYLTHIO)BENZYL BROMIDE 97 can be used to develop new materials with specific properties. The incorporation of this compound into polymers or other materials can result in improved thermal stability, chemical resistance, or other desirable characteristics, depending on the application.
Used in Research and Development:
4-(METHYLTHIO)BENZYL BROMIDE 97 is also used in research and development laboratories for the exploration of new chemical reactions and the development of innovative synthetic methods. Its unique reactivity and structural features make it an interesting candidate for studying various aspects of organic chemistry, including reaction mechanisms, stereochemistry, and catalyst design.

Check Digit Verification of cas no

The CAS Registry Mumber 38185-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,8 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38185-19:
(7*3)+(6*8)+(5*1)+(4*8)+(3*5)+(2*1)+(1*9)=132
132 % 10 = 2
So 38185-19-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H9BrS/c1-10-8-4-2-7(6-9)3-5-8/h2-5H,6H2,1H3

38185-19-2 Well-known Company Product Price

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  • (Code)Product description
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  • Aldrich

  • (634816)  4-(Methylthio)benzylbromide  97%

  • 38185-19-2

  • 634816-1G

  • 338.13CNY

  • Detail
  • Aldrich

  • (634816)  4-(Methylthio)benzylbromide  97%

  • 38185-19-2

  • 634816-5G

  • 1,171.17CNY

  • Detail

38185-19-2Relevant articles and documents

Synthetic Strategy for Tetraphenyl-Substituted All-E-Carotenoids with Improved Molecular Properties

Chung, Wook-Jin,Jung, Hyunuk,Koo, Sangho,Lim, Boram,Park, Myeongnam,Yang, Huijeong,Yoo, Hyebin

, (2020/03/13)

The synthetic method of tetraphenyl-substituted all-E-carotenes 1 with improved properties of antioxidant and molecular electronic conductance was developed through the formation of tetraphenyl-substituted all-E-apocarotenedial 4. The synthesis highlighted the preparation of novel subunits containing phenyl substituent(s) with E-configuration starting from the key (E)-4-chloro-2-phenylbut-2-enal (10), utilizing conjugation effect with formyl group or easy recrystallization of sulfone compounds. Sulfone-mediated coupling methods of Julia and modified Julia–Kocienski olefinations utilizing the subunits were demonstrated to produce tetraphenyl-substituted apocarotenedials 4. The major all-E-forms (73–85 % selectivity) were easily purified by SiO2 chromatography and trituration with Et2O due to the presence of the polar formyl groups. The olefination of all-E-apocarotenedials 4 and Wittig salt 5 provided all-E-9,9',13,13'-tetraphenylcarotenes 1.

Anthranilic acid derivatives as inhibitors of the cGMP-phosphodiesterase

-

, (2008/06/13)

Compounds of formula (I) STR1where R 1 is hydrogen; R 2 is nitro, cyano or halo(lower)alkyl; R 3 is phenyl substituted with one or more substituents selected from halogen, cyano and lower alkoxy; A is a lower alkylene group; R 4 is a group CR 6 R 7 R 8 wherein R 6 and R 7 form, together with the carbon atom to which they are attached a cycloalkyl group optionally substituted with hydroxy, lower alkoxy or a lower alkanoylamino; and R 8 is hydrogen; its prodrug and a salt thereof.

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