5304-21-2
- Product Name：6-Bromo-2-methylbenzo[d]thiazole
- Molecular Formula：C8H6BrNS
- Purity：99%
- Molecular Weight：228.112
Product Details;
CasNo： 5304-21-2
Molecular Formula： C8H6BrNS
factory and supplier 5304-21-2 6-Bromo-2-methylbenzo[d]thiazole in stock
- Molecular Formula:C8H6BrNS
- Molecular Weight:228.112
- Vapor Pressure:0.00217mmHg at 25°C
- Melting Point:82-84 °C
- Refractive Index:1.691
- Boiling Point:299.1 °C at 760 mmHg
- PKA:1.00±0.10(Predicted)
- Flash Point:134.7 °C
- PSA：41.13000
- Density:1.644 g/cm3
- LogP:3.36720
6-BROMO-2-METHYL-1,3-BENZOTHIAZOLE(Cas 5304-21-2) Usage
InChI:InChI=1/C8H6BrNS/c1-5-10-7-3-2-6(9)4-8(7)11-5/h2-4H,1H3
5304-21-2 Relevant articles
-
Naiman,Bogert
, p. 1660,1661 (1935)
-
Recyclable copper-catalyzed cyclization of o-haloanilides and metal sulfides: An efficient and practical access to substituted benzothiazoles
Cai, Mingzhong,Hao, Wenyan,Huang, Wencheng,Ye, Qian
, (2022/01/19)
An efficient heterogeneous copper-cataly...
Di- tert-butyl Peroxide-Mediated Radical C(sp2/sp3)-S Bond Cleavage and Group-Transfer Cyclization
Luo, Kai,Yang, Wen-Chao,Wei, Kai,Liu, Yue,Wang, Jun-Ke,Wu, Lei
supporting information, p. 7851 - 7856 (2019/10/11)
A novel strategy of cascade radical C(sp...
IMIDAZOLIDINONE DERIVATIVES AS INHIBITORS OF PERK
-
Page/Page column 48; 49, (2017/04/11)
The invention is directed to substituted...
RADIOACTIVE IODINE LABELED STYRYL SUBSTITUTED AROMATIC HETEROCYCLIC COMPOUND
-
Paragraph 0055, (2016/11/21)
PROBLEM TO BE SOLVED: To provide a novel...
5304-21-2 Process route
-
-
120-75-2
2-Methylbenzothiazole
-
-
63837-11-6
5-bromo-2-methylbenzothiazole
-
-
5304-21-2
6-bromo-2-methylbenzothiazole
-
-
112146-10-8
4-bromo-2-methyl-1,3-benzothiazole
| Conditions | Yield |
|---|---|
|
With
pyridinium hydrobromide perbromide;
In
water;
|
-
-
562080-91-5
N-(4-bromo-2-iodophenyl)acetamide
-
-
5304-21-2
6-bromo-2-methylbenzothiazole
| Conditions | Yield |
|---|---|
|
N-(4-bromo-2-iodophenyl)acetamide;
With
sodiumsulfide nonahydrate;
In
N,N-dimethyl-formamide;
at 80 ℃;
for 12h;
Schlenk technique;
Sealed tube;
With
hydrogenchloride;
In
N,N-dimethyl-formamide;
at 20 ℃;
for 10h;
|
84% |
|
N-(4-bromo-2-iodophenyl)acetamide;
With
copper(l) iodide; sodiumsulfide nonahydrate;
In
N,N-dimethyl-formamide;
at 80 ℃;
for 12h;
With
hydrogenchloride;
In
N,N-dimethyl-formamide;
at 20 ℃;
|
78% |
|
N-(4-bromo-2-iodophenyl)acetamide;
With
copper(l) iodide; sodiumsulfide nonahydrate;
In
N,N-dimethyl-formamide;
at 80 ℃;
for 12h;
With
hydrogenchloride;
In
water; N,N-dimethyl-formamide;
at 80 ℃;
|
29.5% |
|
N-(4-bromo-2-iodophenyl)acetamide;
With
copper(l) iodide; sodiumsulfide nonahydrate;
In
N,N-dimethyl-formamide;
at 80 ℃;
for 8h;
With
hydrogenchloride;
In
water; N,N-dimethyl-formamide;
at 80 ℃;
for 12h;
|
29.5% |
|
With
copper(l) iodide; sodiumsulfide nonahydrate;
In
N,N-dimethyl-formamide;
at 80 ℃;
for 12h;
|
29.5% |
5304-21-2 Upstream products
-
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6-amino-2-methylbenzothiazole
-
20980-00-1
N-(4-bromophenyl)thioacetamide
-
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(6-bromo-benzothiazol-2-yl)-malonic acid diethyl ester
-
113570-93-7
4-Bromo-2-chlorothioacetanilide
5304-21-2 Downstream products
-
92163-23-0
2-methyl-6-phenoxy-benzothiazole
-
100537-60-8
2-methyl-6-(4-nitro-phenoxy)-benzothiazole
-
100537-47-1
2-methyl-6-(4-nitro-phenylsulfanyl)-benzothiazole
-
107559-02-4
2-methyl-6-phenylbenzothiazole
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