78088-46-7

Basic information

• Product Name: Tabilautide
• Synonyms: Tabilautide
• CAS NO: 78088-46-7
• Molecular Formula: C₂₇H₄₉N₅O₈
• Molecular Weight: 571.711
• Mol File: 78088-46-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 943.4°C at 760 mmHg
• Flash Point: 524.3°C
• Appearance: /
• Density: 1.173g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.519
• CAS DataBase Reference: Tabilautide(CAS DataBase Reference)
• NIST Chemistry Reference: Tabilautide(78088-46-7)
• EPA Substance Registry System: Tabilautide(78088-46-7)

Safety Data

• Hazardous Substances Data: 78088-46-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C27H49N5O8/c1-3-4-5-6-7-8-9-10-11-15-22(33)30-18(2)25(36)32-21(27(39)40)16-17-23(34)31-20(26(37)38)14-12-13-19(28)24(29)35/h18-21H,3-17,28H2,1-2H3,(H2,29,35)(H,30,33)(H,31,34)(H,32,36)(H,37,38)(H,39,40)/t18-,19-,20-,21+/m0/s1

Upstream product

• 41980-31-8 2,6-dicyanopiperidine 
• 41980-32-9 5,5'-trimethylenedihydantoin 
• 112-16-3 n-dodecanoyl chloride 
• 55254-25-6 L-2,6-dibenzyloxycarbonylaminopimelic acid mono p-nitrobenzyl ester 
• 78512-64-8 L-2,6-dibenzyloxycarbonylaminopimelic acid dibenzyl ester 
• 123628-69-3 L-N,N-diphenyl-2,6-dibenzyloxycarbonylaminopimelamide 
• 78147-49-6 L-2,6-dibenzyloxycarbonylaminopimelic acid monobenzyl ester 
• 78057-61-1 L-alanyl-O¹-benzyl-D-glutamic acid hydrochloride 
• 121190-51-0 O¹-p-nitrobenzyl-N²-benzyloxycarbonyl-L-2,6-diaminopimelic acid 
• 78088-48-9 L-2,6-dibenzyloxycarbonylaminopimelamic acid 
• 78057-59-7 O¹-benzyl-N-(N-lauroyl-L-alanyl)-D-glutamic acid 
• 78057-66-6 L-2,6-diaminopimelamic acid dichlorhydrate 
• 78082-26-5 N⁶-benzyloxycarbonyl-L-2,6-diaminopimelamic acid 
• 20714-84-5 L-2,6-dibenzyloxycarbonylaminopimelic acid 

Relevant articles and documents

Synthesis of RP 56142: a New Immunoactive Peptide

RP 56142, a new immunoactive peptide was synthesized on large scale (ca. 500 g) via L-2,6-diaminopimelic acid which was prepared by chemical or biochemical synthesis.The key derivative, N6-benzyloxycarbonyl-L-2,6-diaminopimelamic acid was synthesized by two methods.In the first, we used a copper chelate procedure.In the second, we selectively deblocked the amine at the α-position to the free carboxylic group by the N-carboxyanhydride method.Condensation of N6-benzyloxycarbonyl-L-2,6-diaminopimelamic acid and the appropriately protected lauroyl dipeptide and removal of the protecting groups afforded RP 56142.