Boc-His-OH

Modify Date: 2024-01-02 07:44:22

Boc-His-OH Structure
Boc-His-OH structure
 Common Name Boc-His-OH
CAS Number 17791-52-5 Molecular Weight 255.270
Density 1.3±0.1 g/cm3 Boiling Point 522.2±45.0 °C at 760 mmHg
Molecular Formula C11H17N3O4 Melting Point 195 °C (dec.)(lit.)
MSDS Chinese USA Flash Point 269.6±28.7 °C

 Use of Boc-His-OH


N-tert-Butyloxycarbonyl-L-histidine is a histidine derivative[1].

 Names

Name (2S)-3-(1H-imidazol-5-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
Synonym More Synonyms

 Boc-His-OH Biological Activity

Description N-tert-Butyloxycarbonyl-L-histidine 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.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 522.2±45.0 °C at 760 mmHg
Melting Point 195 °C (dec.)(lit.)
Molecular Formula C11H17N3O4
Molecular Weight 255.270
Flash Point 269.6±28.7 °C
Exact Mass 255.121902
PSA 104.31000
LogP 0.58
Vapour Pressure 0.0±1.4 mmHg at 25°C
Index of Refraction 1.542

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
Risk Phrases R20/21/22
Safety Phrases S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933290090

 Synthetic Route

BOC-HIS(BOM)-OH structure

BOC-HIS(BOM)-OH

CAS#:83468-83-1

~91%

Boc-His-OH Structure

Boc-His-OH

CAS#:17791-52-5
Literature: Tetrahedron Letters, , vol. 43, # 2 p. 311 - 313
Boc-His(Z)-OH structure

Boc-His(Z)-OH

CAS#:50305-43-6

~88%

Boc-His-OH Structure

Boc-His-OH

CAS#:17791-52-5
Literature: Tetrahedron Letters, , vol. 43, # 2 p. 311 - 313
Di-tert-butyl dicarbonate structure

Di-tert-butyl d...

CAS#:24424-99-5

~%

Boc-His-OH Structure

Boc-His-OH

CAS#:17791-52-5
Literature: Chemistry of Natural Compounds, , vol. 18, # 3 p. 322 - 327 Khimiya Prirodnykh Soedinenii, , # 3 p. 349 - 354
L-Histidine structure

L-Histidine

CAS#:71-00-1

~%

Boc-His-OH Structure

Boc-His-OH

CAS#:17791-52-5
Literature: Chemistry of Natural Compounds, , vol. 18, # 3 p. 322 - 327 Khimiya Prirodnykh Soedinenii, , # 3 p. 349 - 354
dicyclohexylamineNa-(tert-butoxycarbonyl)-Nt-((4-methoxy-2,3,6-trimethylphenyl)sulfonyl)-L-histidinate structure

dicyclohexylami...

CAS#:84553-13-9

~%

Boc-His-OH Structure

Boc-His-OH

CAS#:17791-52-5
Literature: Chemical & Pharmaceutical Bulletin, , vol. 30, # 8 p. 2766 - 2779
L-Histidine hydrochloride monohydrate structure

L-Histidine hyd...

CAS#:5934-29-2
BOC-ON structure

BOC-ON

CAS#:58632-95-4

~%

Boc-His-OH Structure

Boc-His-OH

CAS#:17791-52-5
Literature: Chemical and Pharmaceutical Bulletin, , vol. 37, # 11 p. 3112 - 3113
Boc-His(Boc)-OH structure

Boc-His(Boc)-OH

CAS#:20866-46-0

~%

tert-Butyl carbazate structure

tert-Butyl carbazate

CAS#:870-46-2
Boc-His-OH Structure

Boc-His-OH

CAS#:17791-52-5
Literature: Chemistry of Natural Compounds, , vol. 18, # 3 p. 322 - 327 Khimiya Prirodnykh Soedinenii, , # 3 p. 349 - 354
BOC-ON structure

BOC-ON

CAS#:58632-95-4
L-Histidine structure

L-Histidine

CAS#:71-00-1

~%

Boc-His-OH Structure

Boc-His-OH

CAS#:17791-52-5
Literature: Bulletin des Societes Chimiques Belges, , vol. 99, # 10 p. 779 - 782

 Customs

HS Code 2933290090
Summary 2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles2

More Articles
Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Nat. Chem. Biol. 5 , 45-52, (2009)

Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...
Exploring advantages/disadvantages and improvements in overcoming gene delivery barriers of amino acid modified trimethylated chitosan.

Pharm. Res. 32 , 2038-50, (2015)

Present study aimed at exploring advantages/disadvantages of amino acid modified trimethylated chitosan in conquering multiple gene delivery obstacles and thus providing comprehensive understandings f...

 Synonyms

tert-Butyloxycarbonyl-L-histidine
Nalpha-BOC-L-Histidine
n|A-boc-l-histidine
MFCD00065576
Na-(tert-Butoxycarbonyl)-L-histidine
Boc-His-OH
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-histidine
N-Boc-histidine
Nα-(tert-Butoxycarbonyl)-L-histidine
L-Histidine, N-[(1,1-dimethylethoxy)carbonyl]-
Nalpha-(tert-Butoxycarbonyl)-L-histidine
Boc-L-Histidine
N-(tert-Butoxycarbonyl)-L-histidine
EINECS 241-768-9
N-Boc-L-histidine
Nα-boc-L-histidine
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Related Compounds: More...
Boc-His(Bom)-OH
79950-65-5
BOC-HIS(BZL)-OH
20898-44-6
Boc-His(Boc)-OH DCHA
31687-58-8
BOC-HIS(BOM)-OH
83468-83-1
Boc-His(Z)-OH
50305-43-6
Boc-His-Met-OH
248921-84-8
Boc-His(Tos)-OH
35899-43-5
Boc-His(Boc)-OH
20866-46-0
BOC-HIS(DNP)-OH
25024-53-7
Chemsrc provides Boc-His-OH(CAS#:17791-52-5) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of Boc-His-OH are included as well.>> amp version: Boc-His-OH

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