Boc-D-Glu-OBzl

• CAS: 34404-30-3
• Catalog Number: ACM34404303
• Category: Amino Acids
• Molecular Weight: 337.37
• Description: Standard building block for introduction of D-γ-glutamic acid amino-acid residues by Boc SPPS.
• Synonyms: Boc-D-Glu-OBzl, N-α-t.-Boc-D-glutamic acid α-benzyl ester
• InChI: 1S/C17H23NO6/c1-17(2,3)24-16(22)18-13(9-10-14(19)20)15(21)23-11-12-7-5-4-6-8-12/h4-8,13H,9-11H2,1-3H3,(H,18,22)(H,19,20)/t13-/m1/s1
• InChI Key: CVZUKWBYQQYBTF-CYBMUJFWSA-N
• Application: Peptide synthesis.
• Assay: ≥98% (TLC)
• Form: powder
• Functional Group: carboxylic acid
• MDL Number: MFCD00038266
• Quality Level: 200
• Reaction Suitability: reaction type: Boc solid-phase peptide synthesis
• Storage Temperature: 2-8℃

Synthetic Use

Upstream Synthesis Route 1

• 24424-99-5
• 79338-14-0

• 34404-30-3

Reference: [1] Journal of Organic Chemistry, 2015, vol. 80, # 12, p. 6076 - 6082
[2] Patent: JP2015/166329, 2015, A, . Location in patent: Paragraph 0074-0075

Upstream Synthesis Route 2

• 6893-26-1

• 34404-30-3

Reference: [1] Roczniki Chemii, 1974, vol. 48, p. 1921 - 1927

Upstream Synthesis Route 3

• 13303-10-1

• 34404-30-3

Reference: [1] Roczniki Chemii, 1974, vol. 48, p. 1921 - 1927

Upstream Synthesis Route 4

• 100-39-0
• 34404-28-9

• 34404-30-3

Reference: [1]Roczniki Chemii,1974,vol. 48,p. 1921 - 1927

Downstream Synthesis Route 1

• 1738-76-7
• 34404-30-3

• 71822-18-9

Reference: [1]Bulletin of the Chemical Society of Japan,1979,vol. 52,p. 1665 - 1671

* For details of the synthesis route, please refer to the original source to ensure accuracy.