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L-Tyrosine benzyl ester 4-toluenesulfonate
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L-Tyrosine benzyl ester 4-toluenesulfonate

CAS: 53587-11-4

Ref. 3D-FT36700

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Estimated delivery in United States, on Tuesday 21 Jan 2025

Product Information

Name:
L-Tyrosine benzyl ester 4-toluenesulfonate
Synonyms:
  • (S)-Tyrosine benzyl ester tosylate
  • <span class="text-smallcaps">L</span>-Tyrosine benzyl ester 4-methylbenzenesulfonate
  • <span class="text-smallcaps">L</span>-Tyrosine benzyl ester p-toluenesulfonate
  • <span class="text-smallcaps">L</span>-Tyrosine, phenylmethyl ester, 4-methylbenzenesulfonate (1:1)
  • <span class="text-smallcaps">L</span>-Tyrosine, phenylmethyl ester, 4-methylbenzenesulfonate (salt)
  • Benzyl <span class="text-smallcaps">L</span>-tyrosinate tosylate
  • H-Tyr-OBzl*Tos
  • H-Tyr-OBzl.TosOH
  • H-Tyr-OBzl.p-tosylate
  • H-Tyr-OBzl・Tos
  • See more synonyms
  • L-Tyrosine benzyl ester-4-toluenesulfonate
  • Tyr-OBzl.TosOH
  • Tyrosine benzyl ester tosylate
  • Tyrosine benzyl ester tosylate (salt)
  • benzyl L-tyrosinate 4-methylbenzenesulfonate (1:1)
Description:

L-Tyrosine benzyl ester 4-toluenesulfonate is an enantioenriched chiral building block that can be used to synthesize enantiomerically pure compounds. It is a suzuki coupling reaction product of 3-iodo-L-tyrosine and benzyl bromide, which is then reacted with benzenesulfonyl chloride in the presence of triethylamine to give the desired product. The synthesis of L-tyrosine benzyl ester 4-toluenesulfonate has been shown to be more efficient than the traditional method of using L-(+)-leucinamide as the reactant. This process is also advantageous because it does not require the use of a protected amino acid or a protecting group for L-tyrosine.

Notice:
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Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
443.51 g/mol
Formula:
C16H17NO3·C7H8O3S
Purity:
Min. 95%
MDL:
Melting point:
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Concentration:
EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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