1,3-Bis(benzyloxycarbonyl)-2-Methyl-2-thiopseudourea

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Names

[ CAS No. ]:
25508-20-7

[ Name ]:
1,3-Bis(benzyloxycarbonyl)-2-Methyl-2-thiopseudourea

[Synonym ]:
N,N'-dicarbobenzyloxy-S-methylisothiourea
N,N'-di-Cbz-S-methylisothiourea
SMe(C=NCbz)NHCbz
N,N'-dibenzyloxycarbonyl-S-methylisothiourea
1,3-BIS(BENZYLOXYCARBONYL)-2-METHYL-2-THIOPSEUDOUREA
Z2-S-methylisothiourea
1,3-bis(benzoxycarbonyl)-2-methyl-2-thiopseudo urea
1,3-BIS(BENZYLOXYCARBONYL)-2-METHYL-ISOTHIOUREA
MeSC(=NCBz)NHCbz
MFCD00674040
2-Methyl-1,3-di-Z-isothiourea
Carbamic acid, N,N'-[(E)-(methylthio)methylidyne]bis-, bis(phenylmethyl) ester
Dibenzyl [(E)-(methylsulfanyl)methylylidene]biscarbamate
Dibenzyl [(Z)-(methylthio)methylylidene]biscarbamate

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Melting Point ]:
60-63ºC(lit.)

[ Molecular Formula ]:
C18H18N2O4S

[ Molecular Weight ]:
358.411

[ Exact Mass ]:
358.098724

[ PSA ]:
102.29000

[ LogP ]:
4.58

[ Index of Refraction ]:
1.581

[ Storage condition ]:
2-8℃

MSDS

Click to get detail MSDS

Safety Information

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

[ Safety Phrases ]:
S22;S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • S-Methylisothiourea sulfate
  • Benzyl chloroformate
  • METHYL THIOPSEUDOUREA SULFATE
  • Dibenzyl dicarbonate
  • N-(Benzyloxycarbonyloxy)succinimide

DownStream

  • Dibenzyl carbonimidoylbiscarbamate
  • 2-benzyloxycarbonyliminoimidazolidine
  • Benzyl carbamate

Articles

Radiolabeled phenethylguanidines: novel imaging agents for cardiac sympathetic neurons and adrenergic tumors.

J. Med. Chem. 50(9) , 2078-88, (2007)

The norepinephrine transporter (NET) substrates [123I]-m-iodobenzylguanidine (MIBG) and [11C]-m-hydroxyephedrine (HED) are used as markers of cardiac sympathetic neurons and adrenergic tumors (pheochr...

Application of molecular topology to the search of novel NSAIDs: experimental validation of activity. Galvez-Llompart M, et al.

Lett. Drug Des. Discov. 7(6) , 438-445, (2010)

Total synthesis of (+)-batzelladine A and (-)-batzelladine D, and identification of their target protein.

Chemistry 11(23) , 6878-88, (2005)

Asymmetric total synthesis of batzelladine A (1) and batzelladine D (2) has been achieved. Our synthesis of batzelladines features 1) stereoselective construction of the cyclic guanidine system by mea...


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Related Compounds

  • (R)-tert-butyl (1-(3-ethoxyquinoxalin-2-yl)pyrrolidin-3-yl)carbamate
  • Tert-butyl (1-(3-ethoxyquinoxalin-2-yl)piperidin-4-yl)carbamate
  • 2-Chloro-4-(pyrrolidin-3-ylsulfonyl)pyrimidine hydrochloride
  • (R)-tert-butyl 3-((3-ethoxyquinoxalin-2-yl)oxy)piperidine-1-carboxylate
  • tert-Butyl 3-((3-ethoxyquinoxalin-2-yl)oxy)piperidine-1-carboxylate
  • N-(piperidin-3-ylmethyl)-1-(pyridin-4-yl)methanesulfonamide hydrochloride
  • 4-(Piperidin-1-yl)thieno[3,2-d]pyrimidine-6-carboxamide
  • 2-(4,7-Dimethyl-1,3-dioxo-4a,9a-dihydropurino[7,8-a]imidazol-6-yl)acetohydrazide
  • 7-Iodo-5-[(trifluoromethyl)thio]-1,3-benzoxazole
  • tert-butyl N-{[1-(2,2,2-trifluoroethyl)piperidin-4-yl]methyl}carbamate
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