![]() benzyl thiocyanate structure
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Common Name | benzyl thiocyanate | ||
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CAS Number | 3012-37-1 | Molecular Weight | 149.21300 | |
Density | 1.32 | Boiling Point | 230-235 °C(lit.) | |
Molecular Formula | C8H7NS | Melting Point | 39-41 °C(lit.) | |
MSDS | Chinese USA | Flash Point | >230 °F | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
In vitro metabolic conversion of the organic breakdown products of glucosinolate to goitrogenic thiocyanate anion.
J. Sci. Food Agric. 95 , 2244-51, (2015) Glucosinolates are abundant in Brassicaceae vegetables, and they are degraded into various organic breakdown products (BPs) (R-CN, -NCS and -SCN) by myrosinase when plant tissues are damaged. This study was designed to investigate whether these BPs could be b... |
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Subcellular localization of enzymes in Streptomyces aureofaciens and its alteration by benzyl thiocyanate. I. Phosphatases and ATP-glucokinase.
Folia Microbiol. (Praha) 32(5) , 402-10, (1987) Mycelia of a low- and a high-production strain of Streptomyces aureofaciens were converted into protoplasts and divided into five subcellular fractions in order to localize exopolyphosphatases (EC 3.6.1.11), triphosphatase (EC 3.6.1.25), inorganic diphosphata... |
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Protein profiles of Streptomyces aureofaciens producing tetracyclines: reappraisal of the effect of benzyl thiocyanate.
Curr. Microbiol. 31(2) , 84-91, (1995) Cell protein profiles of submerged cultures of Streptomyces aureofaciens cultivated in the absence or presence of 12 microM benzyl thiocyanate (BT) were analyzed by one-dimensional SDS polyacrylamide gel electrophoresis. Substantial increase in the intensity ... |
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Effect of some benzyl thiocyanate analogs on tetracycline production.
J. Antibiot. 40(9) , 1341-3, (1987)
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Effects of dietary compounds on alpha-hydroxylation of N-nitrosopyrrolidine and N'-nitrosonornicotine in rat target tissues.
Cancer Res. 44(7) , 2924-2928, (1984) Male F344 rats were pretreated with various dietary compounds, and the effects of pretreatment on the in vitro alpha-hydroxylation of N-nitrosopyrrolidine or N'-nitrosonornicotine were determined in assays with liver microsomes or cultured esophagus, respecti... |
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Regioselective bond cleavage in the dissociative electron transfer to benzyl thiocyanates.
J. Am. Chem. Soc. 125(42) , 12676-7, (2003) The electrochemical reduction of benzyl thiocyanate and p-nitrobenzyl thiocyanate was investigated in acetonitrile at an inert electrode. These two compounds reveal a change in the reductive cleavage mechanism, and more interestingly, they show a clear-cut ex... |
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Major proteins related to chlortetracycline biosynthesis in a Streptomyces aureofaciens production strain studied by quantitative proteomics.
Appl. Microbiol. Biotechnol. 57(5-6) , 717-24, (2001) Changes in synthesis and abundance of proteins associated with chlortetracycline (CTC) production in Streptomyces aureofaciens were investigated by two-dimensional polyacrylamide gel electrophoresis of proteins pulse-labelled in vivo with L-[35S]methionine. E... |
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Biotransformation of benzyl thiocyanate by Streptomyces aureofaciens.
Lett. Appl. Microbiol. 19(3) , 124-5, (1994) Benzyl thiocyanate, a specific stimulator of chlortetracycline biosynthesis, was transformed into dibenzyl disulphide by Streptomyces aureofaciens. The disulphide stimulated chlortetracycline production to a lesser extent than did benzyl thiocyanate. |
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Palladium-catalyzed, copper(I)-mediated coupling of boronic acids and benzylthiocyanate. A cyanide-free cyanation of boronic acids.
Org. Lett. 8(19) , 4331-3, (2006) A new method for the synthesis of nitriles is described. As a complement to the classic cyanation of aryl halides using cyanide sources and a transition metal catalyst, the palladium-catalyzed cross-coupling of thiocyanates with boronic acids in the presence ... |
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Chemoprevention of colon carcinogenesis by dietary organoselenium, benzylselenocyanate, in F344 rats.
Cancer Res. 47(22) , 5901-4, (1987) The effect of feeding benzylselenocyanate (BSC) and its sulfur analogue, benzylthiocyanate (BTC), 2 wk before, during, and until 1 wk after carcinogen administration (initiation phase) on intestinal carcinogenesis induced by azoxymethane (CAS:25843-45-2) was ... |