DI-TERT-BUTYL (DISULFANEDIYLBIS(ETHANE-2,1-DIYL))DICARBAMATE

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Names

[ CAS No. ]:
67385-10-8

[ Name ]:
DI-TERT-BUTYL (DISULFANEDIYLBIS(ETHANE-2,1-DIYL))DICARBAMATE

[Synonym ]:
di-tert-Butyl (disulfanediylbis(ethane-2,1-diyl))dicarbamate
bis[2-(t-butoxycarbonylamino)]ethyl disulfide
tert-butyl 2,2'-disulfanediylbis(ethane-2,1-diyl)dicarbamate
Di-Boc-cystamine
[2-(2-tert-butoxycarbonylamino-ethylsulfanyl)-thioethyl]carbamic acid tert-butyl ester
N,N-di-(tert-butyloxycarbonyl)-cystamine

Chemical & Physical Properties

[ Density]:
1.128g/cm3

[ Boiling Point ]:
477.2ºC at 760 mmHg

[ Melting Point ]:
120-122ºC

[ Molecular Formula ]:
C14H28N2O4S2

[ Molecular Weight ]:
352.51300

[ Flash Point ]:
242.4ºC

[ Exact Mass ]:
352.14900

[ PSA ]:
127.26000

[ LogP ]:
4.19900

[ Index of Refraction ]:
1.511

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
22-36/37/38

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2930909090

Synthetic Route

Precursor & DownStream

Precursor

  • Di-tert-butyl dicarbonate
  • Cystamine dihydrochloride
  • Cystamine
  • Di-tert-butyl carbonate
  • Ethanamine,2,2'-dithiobis-, hydrochloride (1:1)
  • 2,2′-Dipyridyl disulfide
  • 2-(BOC-Amino)ethanethiol

DownStream

  • 2-(BOC-Amino)ethanethiol
  • TERT-BUTYL 2-(CHLOROSULFONYL)ETHYLCARBAMATE
  • Dimethyl disulfide
  • tert-butyl N-[2-(2-hydroxyethylsulfanyl)ethyl]carbamate

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

A convenient route to thiol terminated peptides for conjugation and surface functionalization strategies.

Bioconjug. Chem. 6 , 323, (1995)

The derivatization of poly(p-(chloromethyl)styrene-co-divinylbenzene) (Merrifield resin) with N-(tert-butoxycarbonyl)-2-aminoethanethiol is presented as a convenient route for the generation of thiol ...

W.J. Moree et al.

Tetrahedron Lett. 49 , 1133, (1993)


More Articles


Related Compounds

  • Methyl 7-formyl-8-hydroxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate
  • 1-Bromo-2-(cyclopropylmethoxy)-4-nitrobenzene
  • 2,2,2-Trifluoro-1-(2,3,4,5-tetramethyl-phenyl)-ethylamine
  • [(5-Chloro-2-iodophenyl)methyl](ethyl)amine
  • (1R)-1-(3-Chlorophenyl)ethane-1,2-diamine
  • Methyl 2-methyl-4-[4-(propan-2-yl)piperidin-1-yl]but-2-enoate
  • (R)-2-(1-Amino-2-hydroxyethyl)-4-methoxyphenol
  • (3E)-5,7-dihydroxy-8-methoxy-3-[(4-methoxyphenyl)methylidene]chromen-4-one
  • (r)-3-(1-Amino-2-hydroxyethyl)benzene-1,2-diol
  • 6-cyano-N-[3-(2-fluorophenyl)-1H-pyrazol-4-yl]pyridine-3-sulfonamide
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