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1074-36-8

  • Product Name4-Mercaptobenzoic acid
  • Molecular FormulaC7H6O2S
  • Molecular Weight154.189
  • Purity99%
  • AppearanceCream colour crystalline solid
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  • CasNo： 1074-36-8
  • Molecular Formula： C7H6O2S
  • Appearance： Cream colour crystalline solid
  • Purity： 99%

Reputable Manufacturer Supply Reliable Quality 4-Mercaptobenzoic acid 1074-36-8 with Cheapest Price

  • Molecular Formula:C7H6O2S
  • Molecular Weight:154.189
  • Appearance/Colour:Cream colour crystalline solid 
  • Vapor Pressure:0.0112mmHg at 25°C 
  • Melting Point:215-224 °C(lit.) 
  • Boiling Point:314.278 °C at 760 mmHg 
  • PKA:4.05±0.10(Predicted) 
  • Flash Point:143.871 °C 
  • PSA：76.10000 
  • Density:1.346 g/cm3 
  • LogP:1.67350 

4-Mercaptobenzoic acid(Cas 1074-36-8) Usage

Chemical Properties

Cream Colour Crystalline Solid

Uses

Gold nanostructures functionalized with 4-Mercaptobenzoic acid (4-MBA) may exhibit improve catalytic activity. Several studies report 4-MBA as a model analyte for surface enhancement Raman scattering (SERS) substrates.

General Description

4-mercaptobenzoic acid (4-MBA) is a probe molecule with thiol and carboxylic groups that form a self-assembled monolayers (SAMs) which can be used for the development of surface enhanced raman spectroscopy (SERS) sensors.

InChI:InChI=1/C7H6O2S/c8-7(9)5-1-3-6(10)4-2-5/h1-4,8-9H/p-2

1074-36-8 Relevant articles

Studies of reversible conjugate additions

Zhong, Ye,Xu, Yufang,Anslyn, Eric V.

, p. 5017 - 5021 (2013)

Benzalcyanoacetamides were designed and ...

Solid phase synthesis of bicyclic pyrrolidines

Quadrelli, Paolo

, (2021/11/17)

The preparation of bicyclic pyrrolidines...

Discovery of 3,5-Dimethyl-4-Sulfonyl-1 H-Pyrrole-Based Myeloid Cell Leukemia 1 Inhibitors with High Affinity, Selectivity, and Oral Bioavailability

Zhu, Peng-Ju,Yu, Ze-Zhou,Lv, Yi-Fei,Zhao, Jing-Long,Tong, Yuan-Yuan,You, Qi-Dong,Jiang, Zheng-Yu

, p. 11330 - 11353 (2021/08/24)

Myeloid cell leukemia 1 (Mcl-1) protein ...

Stabilizing p-Dithiobenzyl Urethane Linkers without Rate-Limiting Self-Immolation for Traceless Drug Release

Zheng, Yiwu,Shen, Yang,Meng, Xiaoting,Wu, Yaqi,Zhao, Yibing,Wu, Chuanliu

, p. 1196 - 1203 (2019/05/28)

Exploiting the redox sensitivity of disu...

Method for synthesizing benzoic acid compound from benzyl alcohol compound by ultrasonic-assisted oxidation

-

Paragraph 0136; 0137, (2018/09/29)

The invention belongs to the field of sy...

1074-36-8 Process route

3-chlorobenzoate
535-80-8

3-chlorobenzoate

4-mercaptobenzoic acid
1074-36-8

4-mercaptobenzoic acid

3-mercapto benzoic acid
4869-59-4

3-mercapto benzoic acid

Conditions
Conditions Yield
With sodium tetrahydroborate; sulfur; Yield given. Multistep reaction. Yields of byproduct given; 1.) 360 deg C, NaOH-KOH melt, 3 min.; 2.) water;
 
4-mercaptobenzyl alcohol
53339-53-0

4-mercaptobenzyl alcohol

4-mercaptobenzoic acid
1074-36-8

4-mercaptobenzoic acid

Conditions
Conditions Yield
With diethylene glycol dimethyl ether; at 70 ℃; for 0.5h; Sonication;
94%
With oxygen; at 120 ℃; for 16h; Green chemistry;
84%

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1074-36-8 Downstream products

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