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
tert-Butyl 6-((tert-butyldimethylsilyl)oxy)-2-nitro-6,7-dihydroimidazo[1,2-a]pyrimidine-8(5H)-carboxylate
4H-1,2,4-Benzothiadiazine-7-carbonitrile, 1,1-dioxide
(S)-2-((tert-Butoxycarbonyl)amino)-3-(1H-indazol-3-yl)propanoic acid
2-Amino-3-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)propanoic acid
2,5-Dichloro-3-[(1-oxopropyl)amino]benzoic acid
2-Amino-5-bromo-3-(trifluoromethyl)phenol
tert-Butyl ethyl(((1r,4r)-4-(hydroxymethyl)cyclohexyl)methyl)carbamate
Methyl 5-acetamido-2-methoxynicotinate
Methyl 2-(4-(tert-butoxycarbonyl(methyl)amino)phenyl)propanoate
3,4-Dimethoxy-N-(4-(3-nitrophenyl)-5-(piperazin-1-ylmethyl)thiazol-2-yl)benzenesulfonamide

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