S-[N-BENZYL(THIOCARBAMOYL)]-L-CYSTEINE

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Names

[ CAS No. ]:
35446-36-7

[ Name ]:
S-[N-BENZYL(THIOCARBAMOYL)]-L-CYSTEINE

[Synonym ]:
Uraton
S-[(benzylamino)carbonothioyl]cysteine
S-<N-benzyl(thiocarbamoyl)>-L-cysteine
Benzylisothiocyanate cysteine conjugate
S-(N-Benzylthiocarbamoyl)cysteine
L-Cysteine (Phenylmethyl)carbamodithioate

Chemical & Physical Properties

[ Density]:
1.363 g/cm3

[ Boiling Point ]:
459.8ºC at 760 mmHg

[ Melting Point ]:
191-193ºC

[ Molecular Formula ]:
C11H14N2O2S2

[ Molecular Weight ]:
270.37100

[ Flash Point ]:
231.9ºC

[ Exact Mass ]:
270.05000

[ PSA ]:
132.74000

[ LogP ]:
2.29740

[ Index of Refraction ]:
1.665

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2930909090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • L-Cysteine hydrochloride anhydrous
  • a-Isothiocyanatotoluene
  • Boc-L-cysteine
  • L-cysteine

DownStream

  • L-cysteine
  • a-Isothiocyanatotoluene

Customs

[ HS Code ]: 2930909090

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Phenylalkyl isothiocyanate-cysteine conjugates as glutathione S-transferase stimulating agents.

J. Med. Chem. 35 , 185, (1992)

To develop analogues of phenylalkyl isothiocyanate with less toxicity and better biological activity, two water-soluble phenylalkyl isothiocyanate-cysteine conjugates, S-[N-benzyl(thiocarbamoyl)]-L-cy...

The metabolism of benzyl isothiocyanate and its cysteine conjugate in guinea-pigs and rabbits.

Xenobiotica 12(9) , 535-42, (1982)

1. Following oral administration of benzyl isothiocyanate or its cysteine conjugate the major metabolite isolated from urine of guinea-pigs and rabbits was a cyclic mercaptopyruvate conjugate, 4-hydro...


More Articles

Related Compounds

  • s-[n-(3-phenylpropyl)(thiocarbamoyl)]-l-cysteine
  • S-benzyl-(L)-cysteine methyl ester
  • S-benzyl-L-cysteine-4-methylcoumarinyl-7-amide
  • N-ACETYL-S-[N-(2-PHENYLETHYL)THIOCARBAMOYL]-L-CYSTEINE
  • N-benzyl-L-leucine methyl ester
  • methyl 2-amino-3-benzylsulfanyl-propanoate
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • tert-Butyl-DL-alanine
  • 4-amino-N-[2-tert-butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]-N-ethylbenzenesulfonamide
  • N-[3-(Aminooxy)propyl]-N-butyl-1-butanamine