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Chinese Manufacturer supply 2-Mercaptobenzoxazole 2382-96-9 in stock with high standard
- Molecular Formula: C7H5NOS
- Molecular Weight: 151.189
- Appearance/Colour: beige crystalline powder
- Vapor Pressure: 0.0258mmHg at 25°C
- Melting Point: 192-195 °C(lit.)
- Refractive Index: 1.714
- Boiling Point: 247.3 °C at 760 mmHg
- PKA: 11.03±0.20(Predicted)
- Flash Point: 103.4 °C
- PSA: 64.83000
- Density: 1.41 g/cm3
- LogP: 2.11650
2-Mercaptobenzoxazole(Cas 2382-96-9) Usage
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Preparation |
2-Mercaptobenzoxazole has already been described in 1876 by Dunner (Ber. 9, (1876) page 465). 2-Mercaptobenzoxazole and its derivatives are prepared by processes which are based in principle on the reaction between o-aminophenol and alkali metal alkylxanthates. The alkali metal alkylxanthate here can either be employed as such, or it can be produced in the reaction mixture itself from an alkali, a lower alkanol and carbon disulphide.https://patents.google.com/patent/US4677209A/en |
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Reactions |
2-Mercaptobenzoxazole with ethyl chloroacetate and anhydrous K2C03 in the presence of dry acetone was refluxed on water bath to give ethyl-2-(mercaptobenzoxazolo)acetate. |
|
Application |
2-Mercaptobenzoxazole is a widely used organic scaffold in medicinal chemistry.2-Mercaptobenzoxazole and their derivatives are known to posses several biological activities such as antibacterial, antifungal, antiinflammatory, insecticidal and herbicidal. 4-0xo-thiazolidines have also played an important activities as analgesic, anti-HIV, antitubercular, anthelmentic, dye-stuffs, fluorescent and as a photosensitizer. The incorporation of 4-oxothiazolidine and their 5-arylidene moieties in 2-mercaptobenzoxazole frame work has been found to enhance the activity. |
InChI:InChI=1/C7H5NOS/c10-7-8-5-3-1-2-4-6(5)9-7/h1-4H,(H,8,10)
2382-96-9 Relevant articles
Photoaddition Reactions of Benzoxazole-2(3H)-thiones to Cycloalkenes and Heteroaromatics
Nishio, Takehiko,Shiwa, Kiyoko,Sakamoto, Masami
, p. 3255 - 3264 (2003)
Photoaddition reactions of benzoxazole-2...
Green synthesis of therapeutically active 1,3,4-oxadiazoles as antioxidants, selective COX-2 inhibitors and their in silico studies
Nesaragi, Aravind R.,Kamble, Ravindra R.,Dixit, Shruti,Kodasi, Barnabas,Hoolageri, Swati R.,Bayannavar, Praveen K.,Dasappa, Jagadeesh Prasad,Vootla, Shyamkumar,Joshi, Shrinivas D.,Kumbar, Vijay M.
supporting information, (2021/06/09)
A modest, competent and green synthetic ...
A green approach for the synthesis of benzazolyl pyrimidinyl carbamothioates under ultrasonication and their antimicrobial activity
Kayathi, Narendra Babu,Panga, Siva Sankar,Adivireddy, Padmaja,Venkatapuram, Padmavathi
, p. 2931 - 2943 (2021/07/26)
A library of benzazolyl pyrimidinyl carb...
Microwave facilitated one-pot three component synthesis of coumarin-benzoxazole clubbed 1,2,3-triazoles: Antimicrobial evaluation, molecular docking and in silico ADME studies
Nesaragi, Aravind R.,Kamble, Ravindra R.,Bayannavar, Praveen K.,Metre, Tukaram V.,Kariduraganavar, Mahadevappa Y.,Margankop, Sheetal B.,Joshi, Shrinivas D.,Kumbar, Vijay M.
, p. 3460 - 3472 (2021/10/02)
4-((4-((Benzo[d]oxazol-2-ylthio)methyl)-...
Synthesis, in?vitro biological screening and docking study of benzo[d]oxazole bis Schiff base derivatives as a potent anti-Alzheimer agent
Alhibshi, Amani H.,Anouar, El Hassane,Khan, Khalid Mohammed,Nawaz, Faisal,Rahim, Fazal,Rehman, Ashfaq Ur,Sajid, Muhammad,Shah, Adnan Ali,Taha, Muhammad,Uddin, Nizam,Wadood, Abdul,Zaman, Khalid
, (2022/01/14)
We have synthesized benzo[d]oxazole deri...
2382-96-9 Process route
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110-89-4
piperidine
-
-
70989-48-9
2-thioxo-benzooxazole-3-carboximidic acid p -tolyl ester
-
-
1530-87-6
1-piperidinylcarbonnitrile
-
-
2382-96-9
benzo[d]oxazole-2-(3H)-thione
-
-
106-44-5
p-cresol
| Conditions | Yield |
|---|---|
|
In
ethanol;
for 0.5h;
Heating;
|
87%
|
-
-
64-17-5
ethanol
-
-
312313-33-0
2-phenyl-1-(2-thioxobenzo[d]oxazol-3(2H)-yl)ethanone
-
-
2382-96-9
benzo[d]oxazole-2-(3H)-thione
-
-
101-97-3
Ethyl 2-phenylethanoate
| Conditions | Yield |
|---|---|
|
In
chloroform-d1;
at 20 ℃;
for 5h;
Irradiation;
|
95 % Spectr.
95 % Spectr. |
2382-96-9 Upstream products
-
1520-26-9
2-hydroxyphenylthiourea
-
615-18-9
2-chloro-1,3-benzoxazole
-
64-17-5
ethanol
-
140-89-6
potassium ethyl xanthogenate
2382-96-9 Downstream products
-
13673-62-6
2-methylsulfanyl-benzoxazole
-
833-50-1
2-phenylbenzo[d]oxazole
-
6296-59-9
2-(benzamido)phenyl benzoate
-
33388-23-7
3-benzoyl-2(3H)-benzoxazolethione
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