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31687-58-8

31687-58-8 structure
31687-58-8 structure
  • Name: Boc-His(Boc)-OH DCHA
  • Chemical Name: N-cyclohexylcyclohexanamine,(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-[1-[(2-methylpropan-2-yl)oxycarbonyl]imidazol-4-yl]propanoic acid
  • CAS Number: 31687-58-8
  • Molecular Formula: C28H48N4O6
  • Molecular Weight: 536.70400
  • Catalog: Biochemical Amino acids and their derivatives Histidine derivative
  • Create Date: 2018-08-01 13:45:41
  • Modify Date: 2026-07-04 20:49:06
  • Boc-His(Boc)-OH.DCHA is a histidine derivative[1].

Name N-cyclohexylcyclohexanamine,(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-[1-[(2-methylpropan-2-yl)oxycarbonyl]imidazol-4-yl]propanoic acid
Synonyms N-ALPHA-N-IM-DI-T-BOC-L-HISTIDINE DICYCLOHEXYLAMMONIUM SALT
N,1-Bis(tert-butoxycbonyl)-L-histidine dicyclohexylamine (1:1)
BOC-HIS(BOC)-OH DCHA //BP
N-cyclohexylcyclohexanamine,(2S)-2-[(2-methylpropan-2-yl)oxycbonylamino]-3-[1-[(2-methylpropan-2-yl)oxycbonyl]imidazol-4-yl]propanoic acid
Boc-His(Z).DCHA
Boc-L-His(Boc)*DCHA
Boc-His(Boc)-OH·DCHA N-α,N-iM-di-Boc-L-histidine dicyclohexylaMine salt
N-α,N-im-di-Boc-L-histidine dicyclohexylamine sal
Boc-His(Boc)-OH·DCHA
N-a-N-im-di-t-Boc-L-Histidinedicyclochexylammoniumsalt
Boc(Nim-Boc)His-OH*DCHA
BOC-HIS(BOC)-OH DCHA
N-α-N-im-di-t-Boc-L-histidine dicyclochexylammonium salt
Boc-His(Boc)-OH. DCHA Novabiochem
N,N-di(tert-butoxycbonyl)-L-histidine dicyclohexylamine
Boc-His(Boc)-OH x DCHA ,(HPLC)
2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-3-[1-[(2-methylpropan-2-yl)oxy-oxomethyl]-4-imidazolyl]propanoic acid
BOC- HS(BOC) -OH DCHA
N-ALPHA,N-IM-DI-T-BUTOXYCBONYL-L-HISTIDINE DICYCLOHEXYLAMMONIUM SALT
BOC-L-HIS(BOC)-OH DCHA
Boc-His(Boc)-OH DCH
(2S)-3-{1-[(tert-butoxy)carbonyl]-1H-imidazol-4-yl}-2-{[(tert-butoxy)carbonyl]amino}propanoic acid
NIM-DI-BOC-L-HISTIDINE DCHA SALT
EINECS 250-764-6
N,N'-Di-Boc-L-histidine dicyclohexylaMMoniuM salt
Boc-His(Boc)-OH (dicyclohexylammonium) salt
N,1-bis(tert-butoxycbonyl)-L-histidine, compound with dicyclohexylamine (1:1)
(Tert-Butoxy)carbonyl His(Boc)-OH·DCHA
N-ALPHA,N-IM-BIS-BOC-L-HISTIDINE DICYCLOHEXYLAMMONIUM SALT
N,1-Bis-Boc-L-histidine DCHA
N-α,N-im-di-Boc-L-histidine dicyclohexylamine salt
Nα,Nim-Bis-Boc-L-histidine dicyclohexylammonium salt
N-S-N(im)-di-tert-Boc-L-histidine dicyclohexylamine salt
NALPHA,Nim-Di-tert-butoxycbonyl-L-histidine dicyclohexylamine salt
Boc-His(Boc)-Ohcha
N-ALPHA-TERT-BUTYLOXYCBONYL-N-IM-TERT-BUTYLOXYCBONYL-L-HISTIDINE DICYCLOHEXYLAMINE
N-ALPHA-T-BUTYLOXYCBONYL-N-IM-T-BUTYLOXYCBONYL-L-HISTIDINE DICYCLOHEXYLAMINE
N-N(im)-di-t-Boc-L-histidineDicyclohexylaminesalt
N,1-Di-Boc-L-histidine dicyclohexylaMMoniuM salt
N-cyclohexylcyclohexanamine,(2S)-2-[(2-methylpropan-2-yl)oxycbonylamino]-3-[1-[(2-methylpropan-2-yl)oxycbonyl]imidazol-4-yl]propanoicaci
N-ALPHA,NIM-DI-BOC-L-HISTIDINE DICYCLOHEXYLAMINE SALT
N-α,N-im-di-Boc-L-histidine
Boc-His(Boc)-OH dicyclohexylamine salt
BOC-NIM-BOC-L-HISTIDINE DICYCLOHEXYLAMINE SALT
Boc-His(Boc).DCHA
Nα,Nim-Bis-Boc-L-histidine dicyclohexylammonium salt (HPLC)
N,1-Bis(Boc)-L-histidine dicyclohexylamine salt
Description Boc-His(Boc)-OH.DCHA is a histidine derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

Boiling Point 679.7ºC at 760 mmHg
Melting Point 160-165ºC (dec.)
Molecular Formula C28H48N4O6
Molecular Weight 536.70400
Flash Point 364.9ºC
Exact Mass 536.35700
PSA 131.78000
LogP 6.20990
Storage condition -20°C
Hazard Codes Xn
Safety Phrases 22-24/25
WGK Germany 3

~75%

31687-58-8 structure

31687-58-8

Literature: Nguyen, Dung Le; Seyer, Rene; Heitz, Annie; Castro, Bertrand Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1985 , p. 1025 - 1032
Precursor  3

DownStream  0

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