31687-58-8

  • Product NameN,1-Di-Boc-L-histidine dicyclohexylammonium salt
  • Molecular FormulaC16H25N3O6.C12H23N
  • Molecular Weight536.712
  • Purity99%
  • AppearanceWhite Powder
Inquiry

Product Details

Quick Details

  • CasNo: 31687-58-8
  • Molecular Formula: C16H25N3O6.C12H23N
  • Appearance: White Powder
  • Purity: 99%

High Quality N,1-Di-Boc-L-histidine dicyclohexylammonium salt 31687-58-8 with Low Price

  • Molecular Formula:C16H25N3O6.C12H23N
  • Molecular Weight:536.712
  • Appearance/Colour:White Powder 
  • Vapor Pressure:2.1E-19mmHg at 25°C 
  • Melting Point:160-165 °C (dec.) 
  • Boiling Point:679.7 °C at 760 mmHg 
  • Flash Point:364.9 °C 
  • PSA:131.78000 
  • LogP:6.20990 

N,1-Di-Boc-L-histidine dicyclohexylammonium salt (Cas 31687-58-8) Usage

Chemical Properties

White powder

Uses N,1-Di-Boc-L-histidine dicyclohexylammonium salt has various applications in the pharmaceutical industry, including as a starting material for the synthesis of various drugs and as a reagent in organic chemistry. It is also used in research studies to investigate the effects of amino acid derivatives on biological systems.

IUPAC Name: N-cyclohexylcyclohexanamine;(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-[1-[(2-methylpropan-2-yl)oxycarbonyl]imidazol-4-yl]propanoic acid  
Isomeric SMILES: CC(C)(C)OC(=O)N[C@@H](CC1=CN(C=N1)C(=O)OC(C)(C)C)C(=O)O.C1CCC(CC1)NC2CCCCC2  
InChIKey: WBGMQHNUPJENDC-MERQFXBCSA-N  
InChI: InChI=1S/C16H25N3O6.C12H23N/c1-15(2,3)24-13(22)18-11(12(20)21)7-10-8-19(9-17-10)14(23)25-16(4,5)6;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h8-9,11H,7H2,1-6H3,(H,18,22)(H,20,21);11-13H,1-10H2/t11-;/m0./s1  

31687-58-8 Relevant articles

l-Histidyl-glycyl-glycyl-l-histidine. Amino-acid structuring of the bleomycin-type pentadentate metal-binding environment capable of efficient double-strand cleavage of plasmid DNA

Satomi Ida a, Kana Iwamaru a, Mikako Fujita b, Yoshinari Okamoto a, Yuri Kudo a, Hiromasa Kurosaki a, Masami Otsuka a

, Bioorganic Chemistry Volume 62, October 2015, Pages 8-14

Boc-His(Boc)-OH·DCHA (1) (2.14 g, 4 mmol) and Gly-OBzl·TsOH (2) (1.34 g, 4 mmol) in acetonitrile (40 mL) under an argon atmosphere. Then, the reaction mixture was stirred at room …

31687-58-8 Process route

di-<i>tert</i>-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

N-cyclohexyl-cyclohexanamine
101-83-7

N-cyclohexyl-cyclohexanamine

L-histidine
71-00-1

L-histidine

Boc-His(Boc)-OH dicyclohexylamine salt
31687-58-8

Boc-His(Boc)-OH dicyclohexylamine salt

Conditions
Conditions Yield
With triethylamine; 1) water, dioxane, 30 to 45 deg C; 2) diethyl ether;
75%
N-[2-N-acetylamino-4-(3-aminophenyl)thiazole]propargylglycinamide

N-[2-N-acetylamino-4-(3-aminophenyl)thiazole]propargylglycinamide

Boc-His(Boc)-OH dicyclohexylamine salt
31687-58-8

Boc-His(Boc)-OH dicyclohexylamine salt

N-[2-N-acetylamino-4-(3-aminophenyl)thiazole]-[Nα,N<sub>imidazole</sub>(di-tert-butoxycarbonyl)]histidylglycinamide

N-[2-N-acetylamino-4-(3-aminophenyl)thiazole]-[Nα,Nimidazole(di-tert-butoxycarbonyl)]histidylglycinamide

Conditions
Conditions Yield
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃;
94%

31687-58-8 Upstream products

  • 24424-99-5
    24424-99-5

    di-tert-butyl dicarbonate

  • 101-83-7
    101-83-7

    N-cyclohexyl-cyclohexanamine

  • 71-00-1
    71-00-1

    L-histidine

31687-58-8 Downstream products

  • 97946-78-6
    97946-78-6

    Nα-t-butoxycarbonyl-Nim-t-butoxycarbonylhistidyl-leucyl-leucylvalyl-O-benzyltyrosyl-O-benzylserine benzyl ester

;