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Ethyl-7-nitro-5-(trifluoromethyl)-2-benzothiazole carboxylate is a nitrobenzothiazole derivative with a trifluoromethyl group attached to the benzene ring, featuring the molecular formula C13H8F3N2O4S.
Used in Biomedical Applications:
Ethyl-7-nitro-5-(trifluoroMethyl)-2-benzothiazole carboxylate is used as a fluorescent probe for detecting and measuring the presence of lipid hydroperoxides in biological systems.
Used in Biomedical Imaging:
Ethyl-7-nitro-5-(trifluoroMethyl)-2-benzothiazole carboxylate is used as a potential tool in biomedical imaging, aiding in the visualization of biological processes.
Used in Cancer Research:
Ethyl-7-nitro-5-(trifluoroMethyl)-2-benzothiazole carboxylate is used as a compound in cancer research, potentially contributing to the development of new diagnostic or therapeutic approaches.
Used in Antimicrobial Applications:
Ethyl-7-nitro-5-(trifluoroMethyl)-2-benzothiazole carboxylate is used as an antimicrobial agent, being investigated for its potential in the development of new drugs to combat microbial infections.

40160-42-7

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40160-42-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40160-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,6 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40160-42:
(7*4)+(6*0)+(5*1)+(4*6)+(3*0)+(2*4)+(1*2)=67
67 % 10 = 7
So 40160-42-7 is a valid CAS Registry Number.

40160-42-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzo-thiazole-2-carboxylate

1.2 Other means of identification

Product number -
Other names ETHYL 7-NITRO-5-(TRIFLUOROMETHYL)-1,3-BENZOTHIAZOLE-2-CARBOXYLATE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:40160-42-7 SDS

40160-42-7Synthetic route

ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzothiazole-2-carboxylate-3-oxide
34576-35-7

ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzothiazole-2-carboxylate-3-oxide

ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzo-thiazole-2-carboxylate
40160-42-7

ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzo-thiazole-2-carboxylate

Conditions
ConditionsYield
With triethyl phosphite In ethanol at 20 - 70℃; for 2h;16.98 g
ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzo-thiazole-2-carboxylate
40160-42-7

ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzo-thiazole-2-carboxylate

2-carbamoyl-7-nitro-5-(trifluoromethyl)benzothiazole
40160-50-7

2-carbamoyl-7-nitro-5-(trifluoromethyl)benzothiazole

Conditions
ConditionsYield
With ammonia In methanol
ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzo-thiazole-2-carboxylate
40160-42-7

ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzo-thiazole-2-carboxylate

7-nitro-5-trifluoromethyl-benzothiazole-2-carbonitrile
40160-64-3

7-nitro-5-trifluoromethyl-benzothiazole-2-carbonitrile

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: NH3 / methanol
2: POCl3 / 1 h / 110 °C
View Scheme
[2-(2-thyenyl)ethyl]amine
30433-91-1

[2-(2-thyenyl)ethyl]amine

ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzo-thiazole-2-carboxylate
40160-42-7

ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzo-thiazole-2-carboxylate

7-nitro-N-(2-thien-2-ylethyl)-5-(trifluoromethyl)-1,3-benzothiazole-2-carboxamide
1376938-98-5

7-nitro-N-(2-thien-2-ylethyl)-5-(trifluoromethyl)-1,3-benzothiazole-2-carboxamide

Conditions
ConditionsYield
In methanol; N,N-dimethyl-formamide at 20℃;
4-(2-aminoethyl)tetrahydropyran
65412-03-5

4-(2-aminoethyl)tetrahydropyran

ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzo-thiazole-2-carboxylate
40160-42-7

ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzo-thiazole-2-carboxylate

7-nitro-N-[2-(tetrahydro-2H-pyran-4-yl)ethyl]-5-(trifluoromethyl)-1,3-benzothiazole-2-carboxamide
1376938-66-7

7-nitro-N-[2-(tetrahydro-2H-pyran-4-yl)ethyl]-5-(trifluoromethyl)-1,3-benzothiazole-2-carboxamide

Conditions
ConditionsYield
In methanol at 20℃; for 18h;0.081 g
ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzo-thiazole-2-carboxylate
40160-42-7

ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzo-thiazole-2-carboxylate

trifluoroacetic acid
76-05-1

trifluoroacetic acid

2-(3-chlorophenyl)ethylamine
13078-79-0

2-(3-chlorophenyl)ethylamine

N-[2-(3-chlorophenyl)ethyl]-7-nitro-5-(trifluoromethyl)-1,3-benzothiazole-2-carboxamide trifluoroacetic acid salt

N-[2-(3-chlorophenyl)ethyl]-7-nitro-5-(trifluoromethyl)-1,3-benzothiazole-2-carboxamide trifluoroacetic acid salt

Conditions
ConditionsYield
Stage #1: ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzo-thiazole-2-carboxylate; 2-(3-chlorophenyl)ethylamine In methanol; N,N-dimethyl-formamide at 20℃;
Stage #2: trifluoroacetic acid In N,N-dimethyl-formamide

40160-42-7Downstream Products

40160-42-7Relevant academic research and scientific papers

NITROBENZOTHIAZOLE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC APPLICATIONS THEREOF

-

Paragraph 0127, (2013/09/26)

The invention relates to the nitrobenzothiazole derivatives of general formula (I): and to the use thereof for treating tuberculosis.

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