Boc-Tyr(Bzl)-OH

• CAS: 2130-96-3
• Catalog Number: ACM2130963-1
• Category: Amino Acids
• Molecular Weight: 371.43
• Description: Building block for introduction of tyrosine amino-acid residues by Boc SPPS.
• Synonyms: Boc-Tyr(Bzl)-OH, N-α-t.-Boc-O-benzyl-L-tyrosine
• InChI: 1S/C21H25NO5/c1-21(2,3)27-20(25)22-18(19(23)24)13-15-9-11-17(12-10-15)26-14-16-7-5-4-6-8-16/h4-12,18H,13-14H2,1-3H3,(H,22,25)(H,23,24)
• InChI Key: ZAVSPTOJKOFMTA-UHFFFAOYSA-N
• Application: Peptide synthesis.
• Assay: ≥98% (TLC); ≥98.0% (HPLC)
• Form: powder
• Functional Group: hydroxyl
• MDL Number: MFCD00065597
• Quality Level: 200
• Reaction Suitability: reaction type: Boc solid-phase peptide synthesis
• Storage Temperature: 2-30℃

Synthetic Use

Upstream Synthesis Route 1

• 3978-80-1
• 100-39-0

• 2130-96-3

Reference: [1] Patent: US2005/283021, 2005, A1, . Location in patent: Page/Page column 6

Upstream Synthesis Route 2

• 3978-80-1
• 100-44-7

• 2130-96-3

Reference: [1] Patent: US2005/283021, 2005, A1, . Location in patent: Page/Page column 6

Upstream Synthesis Route 3

• 24424-99-5
• 100-39-0
• 60-18-4

• 2130-96-3

Reference: [1] Patent: EP2133342, 2009, A1, . Location in patent: Page/Page column 32

Upstream Synthesis Route 4

• 16652-64-5

• 2130-96-3

Reference: [1]Helvetica Chimica Acta,1959,vol. 42,p. 2622

Upstream Synthesis Route 5

• 1070-19-5
• 16652-64-5

• 2130-96-3

Reference: [1]Monatshefte fur Chemie,1974,vol. 105,p. 1110 - 1135
[2]Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry,1977,vol. 15,p. 80 - 81

Upstream Synthesis Route 6

• 16965-08-5
• 16652-64-5

• 2130-96-3

Reference: [1]Journal of the Chemical Society C: Organic,1967,p. 2632 - 2636