71591-33-8

Basic information

• Product Name: Carbamic acid, [2-azido-1-[(4-hydroxyphenyl)methyl]-2-oxoethyl]-, 1,1-dimethylethyl ester, (S)-
• CAS NO: 71591-33-8
• Molecular Formula: C14H18N4O4
• Molecular Weight: 306.321
• Mol File: 71591-33-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [2-azido-1-[(4-hydroxyphenyl)methyl]-2-oxoethyl]-, 1,1-dimethylethyl ester, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [2-azido-1-[(4-hydroxyphenyl)methyl]-2-oxoethyl]-, 1,1-dimethylethyl ester, (S)-(71591-33-8)
• EPA Substance Registry System: Carbamic acid, [2-azido-1-[(4-hydroxyphenyl)methyl]-2-oxoethyl]-, 1,1-dimethylethyl ester, (S)-(71591-33-8)

Safety Data

• Hazardous Substances Data: 71591-33-8(Hazardous Substances Data)

Upstream product

• 3978-80-1 Boc-Tyr-OH 
• 23506-20-9 tert-butyl (1-hydrazinyl-3-(4-hydroxyphenyl)-1-oxopropan-2-yl)carbamate 

Downstream Products

• 1051456-03-1 C₁₈H₂₃N₃O₇ 
• 131696-84-9 H-Tyr-Asn-Pro-Gly-OMe*HCl 
• 83579-08-2 H-Tyr-D-Ala-Phe-Gly-NH-Ad 
• 16874-55-8 Boc-Tyr-Ser-NHNH₂ 
• 86961-32-2 Boc-Tyr-Leu-Val-CH₂Cl 
• 86961-32-2 Boc-Tyr-Leu-D-Val-CH₂Cl 
• 86961-32-2 Boc-Tyr-D-Leu-Val-CH₂Cl 
• 86961-32-2 Boc-Tyr-D-Leu-D-Val-CH₂Cl 
• 112372-42-6 Boc-Asp(OBzl)-Tyr-Pro-OH 
• 51871-47-7 H-Tyr-Pro-OH 
• 92465-90-2 Boc-Tyr-Cys(MBzl)-Cys(MBzl)-Glu(OBu^t)-Leu-OEt 
• 92465-91-3 Boc-Tyr-Cys(MBzl)-Cys(MBzl)-Glu(OBu^t)-Leu-N₂H₃ 
• 92465-89-9 Boc-Tyr-Cys(MBzl)-Cys(MBzl)-N₂H₃ 
• 627535-20-0 3,6-bis[2'-(N^α-Boc-Tyr)aminoethyl]-5-methyl-2(1H)-pyrazinone 

Relevant articles and documents

Efficient synthesis of O-succinimidyl-(tert-butoxycarbonylamino)methyl carbamates derived from α-amino acids accelerated by ultrasound: Application to the synthesis of ureidodipeptides

The synthesis of O-succinimidyl-(tert-butoxycarbonylamino)methyl carbamates employing isocyanates made through the Curtius rearrangement of Boc-amino acid azides in the presence of N-hydroxysuccinimide under the influence of ultrasound is described. Copyright Taylor & Francis Group, LLC.

Amino acids and peptides. XXVIII. Synthesis of peptide fragments related to eglin c and studies on the relationship between their structure and effects on human leukocyte elastase, cathepsin G and α-chymotrypsin

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Studies on α2-plasmin inhibitor fragment T-11. I. Synthesis of the protected hexadecapeptide ester corresponding to positions 11 through 26 of α2-plasmin inhibitor fragment T-11

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