Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H7NS |
| Molecular Weight | 149.213 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
N#CSCC1=CC=CC=C1
InChI
InChIKey=ABNDFSOIUFLJAH-UHFFFAOYSA-N
InChI=1S/C8H7NS/c9-7-10-6-8-4-2-1-3-5-8/h1-5H,6H2
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Validation of Different Methods of Preparation of Adhatoda vasica Leaf Juice by Quantification of Total Alkaloids and Vasicine. | 2008-01 |
|
| Palladium-catalyzed, copper(I)-mediated coupling of boronic acids and benzylthiocyanate. A cyanide-free cyanation of boronic acids. | 2006-09-14 |
|
| Phenethyl isothiocyanate triggers apoptosis in Jurkat cells made resistant by the overexpression of Bcl-2. | 2006-07-01 |
|
| Regioselective bond cleavage in the dissociative electron transfer to benzyl thiocyanates: the role of radical/ion pair formation. | 2006-05-24 |
|
| Structure-activity relationship of S-benzylisothiourea derivatives to induce spherical cells in Escherichia coli. | 2004-11 |
|
| Regioselective bond cleavage in the dissociative electron transfer to benzyl thiocyanates. | 2003-10-22 |
|
| Involvement of toxicity as an early event in urinary bladder carcinogenesis induced by phenethyl isothiocyanate, benzyl isothiocyanate, and analogues in F344 rats. | 2003-07-10 |
|
| Composition of the essential oil of Lepidium meyenii (Walp). | 2002-09 |
|
| Preparation of 2,6-dimethyl-4-arylpyridine- 3,5-dicarbonitrile: a paired electrosynthesis. | 2002-04-05 |
|
| Major proteins related to chlortetracycline biosynthesis in a Streptomyces aureofaciens production strain studied by quantitative proteomics. | 2001-12 |
|
| Benzyl isothiocyanate is the chief or sole anthelmintic in papaya seed extracts. | 2001-06 |
|
| Polarographic investigation of reduction process of some azodyes and their complexes with rare earths. | 2001-04-12 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID5020156
Created by
admin on Mon Mar 31 19:22:47 GMT 2025 , Edited by admin on Mon Mar 31 19:22:47 GMT 2025
|
PRIMARY | |||
|
16017
Created by
admin on Mon Mar 31 19:22:47 GMT 2025 , Edited by admin on Mon Mar 31 19:22:47 GMT 2025
|
PRIMARY | |||
|
130266
Created by
admin on Mon Mar 31 19:22:47 GMT 2025 , Edited by admin on Mon Mar 31 19:22:47 GMT 2025
|
PRIMARY | |||
|
100000077161
Created by
admin on Mon Mar 31 19:22:47 GMT 2025 , Edited by admin on Mon Mar 31 19:22:47 GMT 2025
|
PRIMARY | |||
|
C034658
Created by
admin on Mon Mar 31 19:22:47 GMT 2025 , Edited by admin on Mon Mar 31 19:22:47 GMT 2025
|
PRIMARY | |||
|
YX8TAO9O90
Created by
admin on Mon Mar 31 19:22:47 GMT 2025 , Edited by admin on Mon Mar 31 19:22:47 GMT 2025
|
PRIMARY | |||
|
221-144-2
Created by
admin on Mon Mar 31 19:22:47 GMT 2025 , Edited by admin on Mon Mar 31 19:22:47 GMT 2025
|
PRIMARY | |||
|
3012-37-1
Created by
admin on Mon Mar 31 19:22:47 GMT 2025 , Edited by admin on Mon Mar 31 19:22:47 GMT 2025
|
PRIMARY | |||
|
1729
Created by
admin on Mon Mar 31 19:22:47 GMT 2025 , Edited by admin on Mon Mar 31 19:22:47 GMT 2025
|
PRIMARY | |||
|
SUB13028MIG
Created by
admin on Mon Mar 31 19:22:47 GMT 2025 , Edited by admin on Mon Mar 31 19:22:47 GMT 2025
|
PRIMARY | |||
|
18170
Created by
admin on Mon Mar 31 19:22:47 GMT 2025 , Edited by admin on Mon Mar 31 19:22:47 GMT 2025
|
PRIMARY |
SUBSTANCE RECORD