Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H6S |
| Molecular Weight | 74.145 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
SCC=C
InChI
InChIKey=ULIKDJVNUXNQHS-UHFFFAOYSA-N
InChI=1S/C3H6S/c1-2-3-4/h2,4H,1,3H2
| Molecular Formula | C3H6S |
| Molecular Weight | 74.145 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Molecular gastronomy: a new emerging scientific discipline. | 2010-04-14 |
|
| Novel derivatives of 6-mercaptopurine: synthesis, characterization and antiproliferative activities of S-allylthio-mercaptopurines. | 2009-02 |
|
| Selective chain reaction of acetone leading to the successive growth of mutually perpendicular molecular lines on the si(100)-(2 x 1)-H surface. | 2007-10-10 |
|
| Studies on the deodorization by mushroom (Agaricus bisporus) extract of garlic extract-induced oral malodor. | 2007-06 |
|
| A novel monolithic column for capillary electrochromatographic separation of oligopeptides. | 2006-07-21 |
|
| Preparation of new nitrogen-bridged heterocycles. 58. Syntheses and intramolecular arene-pi interactions of 3-(allylthio)- and 3-(propargylthio)thieno[3,4-b]indolizine derivatives. | 2005-11 |
|
| Synthesis of 3-alkylthio-6-allylthiopyridazine derivatives and their antihepatocarcinoma activity. | 2005-04 |
|
| Synthesis of the flavour precursor, alliin, in garlic tissue cultures. | 2005-01 |
|
| Synthesis and NMR spectroscopic studies of allylsulfanyl-N1-alkyl-N4-phenyl-1,4-phenylenediamines and their cyclization products, 2,3-dihydro-1-benzothiophenes and thiochromans. | 2004-12 |
|
| Deodorization with ku-ding-cha containing a large amount of caffeoyl quinic acid derivatives. | 2004-08-25 |
|
| Absolute rate constants for reactions of tributylstannyl radicals with bromoalkanes, episulfides, and alpha-halomethyl-episulfides, -cyclopropanes, and -oxiranes: new rate expressions for sulfur and bromine atom abstraction. | 2004-02-20 |
|
| Hepatic metabolism of diallyl disulphide in rat and man. | 2003-12 |
|
| Thioepoxide formation by ring closure of allylthiyl radicals--a novel rearrangement of allylic thionitrites. | 2002-10-21 |
|
| Effects of food materials on removal of Allium-specific volatile sulfur compounds. | 2002-06-19 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:48:13 GMT 2025
by
admin
on
Mon Mar 31 18:48:13 GMT 2025
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| Record UNII |
1X587IBY09
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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| Classification Tree | Code System | Code | ||
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CFR |
21 CFR 172.515
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JECFA EVALUATION |
ALLYL MERCAPTAN
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NCI_THESAURUS |
C68520
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59723
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212-792-7
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DTXSID2061226
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870-23-5
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Allyl mercaptan
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1X587IBY09
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13367
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C68522
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6744
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131
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