Chemodex

(Boc-Cys-OH)2

Product Code:
 
CDX-B0224
Product Group:
 
Other Biochemicals
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
+4°C
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Chemical Structure
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Chemical Structure

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CDX-B0224-G0055 g£78.00
Quantity:
CDX-B0224-G02525 g£280.00
Quantity:
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This product comes from: Switzerland.
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Further Information

Alternate Names/Synonyms:
Nalp. Nalp.'-di-Boc-L-cystine; N,N'-Di(tert-butoxycarbonyl)-L-cystine; NSC 164046
Appearance:
White powder.
CAS:
10389-65-8
EClass:
32160000
Form (Short):
liquid
Handling Advice:
Keep cool and dry.Protect from light and moisture.
InChi:
InChI=1S/C16H28N2O8S2/c1-15(2,3)25-13(23)17-9(11(19)20)7-27-28-8-10(12(21)22)18-14(24)26-16(4,5)6/h9-10H,7-8H2,1-6H3,(H,17,23)(H,18,24)(H,19,20)(H,21,22)/t9-,10-/m0/s1
InChiKey:
MHDQAZHYHAOTKR-UWVGGRQHSA-N
Long Description:
Chemical. CAS: 10389-65-8. Formula: C16H28N2O8S2. MW: 440.53. Synthetic. Amino acid protected by tert-butoxycarbonyl (Boc) group. Used as a reactant in peptide synthesis. Used to obtain asymmetric cystine peptides by enzymatic catalysis with immobilized papain. Used as educt for obtaining S-isoacyl dipeptide building blocks.
MDL:
MFCD00038250
Molecular Formula:
C16H28N2O8S2
Molecular Weight:
440.53
Package Type:
Vial
Product Description:
Amino acid protected by tert-butoxycarbonyl (Boc) group. Used as a reactant in peptide synthesis. Used to obtain asymmetric cystine peptides by enzymatic catalysis with immobilized papain. Used as educt for obtaining S-isoacyl dipeptide building blocks.
Purity:
>98% (CE)
SMILES:
CC(C)(C)OC(=O)N[C@@H](CSSC[C@H](NC(=O)OC(C)(C)C)C(O)=O)C(O)=O
Solubility Chemicals:
Soluble in acetone or ethanol.
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

References

(1) O. Keller, et al.; Org. Synth. 63, 160 (1985) | (2) D.-F. Tai, et al.; Biotechnol. Lett. 15, 961 (1993) | (3) D.-F. Tai, et al.; Bioorg. Med. Chem. Lett. 5, 1475 (1995) | (4) T. Yoshiya, et al.; J. Pept. Sci. 14, 1203 (2008)