3274-73-5

Basic information

• Product Name: S-benzyl-N-(benzyloxycarbonyl)-L-cysteinyl-L-tyrosyl-L-isoleucyl-L-glutaminyl-L-asparaginyl-S-benzyl-L-cysteinyl-L-prolyl-L-leucylglycinamide
• Synonyms: S-benzyl-N-(benzyloxycarbonyl)-L-cysteinyl-L-tyrosyl-L-isoleucyl-L-glutaminyl-L-asparaginyl-S-benzyl-L-cysteinyl-L-prolyl-L-leucylglycinamide;N-Cbz-S-Bzl-Cys-L-Tyr-L-Ile-L-Gln-L-Asn-S-Bzl-L-Cys-L-Pro-L-Leu-Gly-NH2;Z-S-Bzl-L-Cys-L-Tyr-L-Ile-L-Gln-L-Asn-S-Bzl-L-Cys-L-Pro-L-Leu-Gly-NH2
• CAS NO: 3274-73-5
• Molecular Formula: C₆₅H₈₆N₁₂O₁₄S₂
• Molecular Weight: 1323.58034
• EINECS: 221-903-8
• Mol File: 3274-73-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 1622.2°Cat760mmHg
• Flash Point: 934.9°C
• Appearance: /
• Density: 1.299g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.603
• CAS DataBase Reference: S-benzyl-N-(benzyloxycarbonyl)-L-cysteinyl-L-tyrosyl-L-isoleucyl-L-glutaminyl-L-asparaginyl-S-benzyl-L-cysteinyl-L-prolyl-L-leucylglycinamide(CAS DataBase Reference)
• NIST Chemistry Reference: S-benzyl-N-(benzyloxycarbonyl)-L-cysteinyl-L-tyrosyl-L-isoleucyl-L-glutaminyl-L-asparaginyl-S-benzyl-L-cysteinyl-L-prolyl-L-leucylglycinamide(3274-73-5)
• EPA Substance Registry System: S-benzyl-N-(benzyloxycarbonyl)-L-cysteinyl-L-tyrosyl-L-isoleucyl-L-glutaminyl-L-asparaginyl-S-benzyl-L-cysteinyl-L-prolyl-L-leucylglycinamide(3274-73-5)

Safety Data

• Hazardous Substances Data: 3274-73-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C65H86N12O14S2/c1-5-40(4)56(76-60(85)48(31-41-23-25-45(78)26-24-41)71-61(86)50(37-92-35-43-18-11-7-12-19-43)75-65(90)91-34-42-16-9-6-10-17-42)63(88)70-46(27-28-53(66)79)58(83)72-49(32-54(67)80)59(84)74-51(38-93-36-44-20-13-8-14-21-44)64(89)77-29-15-22-52(77)62(87)73-47(30-39(2)3)57(82)69-33-55(68)81/h6-14,16-21,23-26,39-40,46-52,56,78H,5,15,22,27-38H2,1-4H3,(H2,66,79)(H2,67,80)(H2,68,81)(H,69,82)(H,70,88)(H,71,86)(H,72,83)(H,73,87)(H,74,84)(H,75,90)(H,76,85)/t40?,46-,47-,48-,49-,50-,51-,52-,56-/m0/s1

Upstream product

• 29022-11-5 N-(fluoren-9-ylmethoxycarbonyl)glycine 

Downstream Products

• 50-56-6 oxytocin 

Relevant articles and documents

Fluorenylmethoxycarbonylamino Acid Active Esters in Solid Phase Peptide Synthesis Using p-Alkoxybenzyl Alcohol Resin: Synthesis of Oxytocin

A superior solid phase synthesis of the pituitary hormone, oxytocin (I) has been accomblished by the condensation of fluorenylmethoxycarbonyl(Fmoc)-amino acid active esters in the presence of 1-hydroxybenzotriazole (HOBt)