Boc-Tyr(OAllyl)-OH

Names

[ CAS No. ]:
127132-38-1

[ Name ]:
Boc-Tyr(OAllyl)-OH

[Synonym ]:
Boc-O-allyl-L-tyrosine
BOC-O-ALLYL-L-TYROSINE
BOC-L-TYROSINE ALLYL ESTER

Chemical & Physical Properties

[ Density]:
1.145 g/cm3

[ Boiling Point ]:
490.39ºC at 760 mmHg

[ Melting Point ]:
76-77 °C

[ Molecular Formula ]:
C₁₇H₂₃NO₅

[ Molecular Weight ]:
321.36800

[ Exact Mass ]:
321.15800

[ PSA ]:
84.86000

[ LogP ]:
3.16270

[ Vapour Pressure ]:
0mmHg at 25°C

[ Index of Refraction ]:
1.526

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2924299090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

(S)-Ethyl 3-(4-(allyloxy)phenyl)-2-((tert-butoxycarbonyl)amino) propanoate
Boc-Tyr-OH
allyl bromide
Di-tert-butyl dicarbonate
Ethyl L-tyrosinate
Boc-Tyr-Oet

DownStream

Boc-Tyr-OH
N-(trifluoroacetyl)valyl-O'-(2,3-epoxypropyl)tyrosyl-valine methyl ester

Customs

[ HS Code ]: 2924299090

[ Summary ]:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Allyl-based groups for side-chain protection of amino-acids.

Int. J. Pept. Protein Res. 42 , 346, (1993)

Allyl and allyloxycarbonyl groups are used for the side-chain protection of amino acids. The protecting groups may be selectively cleaved using the reagent HSnBu3 under palladium catalysis. The prepar...

Angew. Chem. Int. Ed. Engl. 114 , 2964, (2002)

Boc-[Tyr(OH)]3-OBn
BOC-TYR-OH DCHA
Boc-[Tyr(OH)]2-OBn
Boc-Tyr-OH
BOC-TYR(BZL)-OH
Boc-Tyr-Pro-OH
2-cyano-N-(2,5-dichlorophenyl)-3-(4-hydroxyphenyl)prop-2-enamide
3-{2-chloroimidazo[1,2-a]pyridin-3-yl}-2-cyano-N-(4-methoxyphenyl)prop-2-enamide
N-benzyl-3-(1-benzyl-5-chloro-3-methyl-1H-pyrazol-4-yl)-2-cyanoprop-2-enamide
9-Chloro-10-phenylanthracene
[5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl]methyl 5,6-dichloropyridine-3-carboxylate
[2-[(1-Methoxy-1-oxo-3-phenylpropan-2-yl)amino]-2-oxoethyl] 4-formylbenzoate
2-[(2-Methoxy-5-methylphenyl)amino]acetamide
5-methyl-5-(naphthalen-2-yl)-3-(2-oxo-2-(4-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidin-1-yl)ethyl)imidazolidine-2,4-dione
1-[4-(2-fluorobenzenesulfonyl)piperazin-1-yl]-2-({1-[(oxolan-2-yl)methyl]-1H-1,2,3,4-tetrazol-5-yl}sulfanyl)ethan-1-one
2-({5-[(2-methyl-1,3-thiazol-4-yl)methyl]-1,3,4-oxadiazol-2-yl}sulfanyl)-N-[2-(1H-1,2,4-triazol-1-yl)-5-(trifluoromethyl)phenyl]acetamide

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