Tevcv

Base Information

Chemical Name:Tevcv
CAS No.:92954-83-1
Molecular Formula:C₅₃H₇₆N₁₂O₁₂S₂
Molecular Weight:1137.39
Hs Code.:

Synonyms:(beta mercapto-beta,beta-cyclopentamethylenepropionic acid)-2-(O-Et-Tyr)-4-Val-8-Cit vasopressin;d(CH2)5Tyr(OEt)2,Val(4),Cit(8) vasopressin;TEVCV;vasopressin, beta-mercapto beta,beta-cyclopentamethylenepropionic acid(1)-O-ethyl-Tyr(2)-Val(4)-Cit(8)-;vasopressin,beta-mercapto beta,beta-cyclopentamethylenepropionic acid(1)-O-ethyltyrosyl(2)-valyl(4)-citrulline(8)-

Suppliers and Price of Tevcv

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of Tevcv

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:1520.7°Cat760mmHg
Flash Point:873.5°C
PSA：425.14000
Density:1.36g/cm³
LogP:4.69520
XLogP3:0.7
Hydrogen Bond Donor Count:11
Hydrogen Bond Acceptor Count:14
Rotatable Bond Count:19
Exact Mass:1136.51470825
Heavy Atom Count:79
Complexity:2140

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC1=CC=C(C=C1)CC2C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(CSSC3(CCCCC3)CC(=O)N2)C(=O)N4CCCC4C(=O)NC(CCCNC(=O)N)C(=O)NCC(=O)N)CC(=O)N)C(C)C)CC5=CC=CC=C5
Isomeric SMILES:CCOC1=CC=C(C=C1)C[C@@H]2C(=O)N[C@@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](CSSC3(CCCCC3)CC(=O)N2)C(=O)N4CCC[C@H]4C(=O)NC(CCCNC(=O)N)C(=O)NCC(=O)N)CC(=O)N)C(C)C)CC5=CC=CC=C5

Technology Process of Tevcv

There total 4 articles about Tevcv which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 117710-49-3
<β-(benzylthio)-β,β-pentamethylenepropionyl>-D-Tyr(Et)-Phe-Val-Asn-Cys(Bzl)-Pro-Cit-Gly-NH2

: 92954-83-1
<1-(β-mercapto-β,β-pentamethylenepropionic acid),2-O-ethyl-D-tyrosine,4-valine,8-citrulline>vasopressin

Guidance literature:: With sodium; potassium hexacyanoferrate(III); Yield given. Multistep reaction; 1.) liquid ammonia, reflux, 2.) water, pH=7, 20 min;
DOI:10.1021/jm00122a016

Reference yield:

: 15761-39-4,59433-50-0
1-(tert-butoxycarbonyl)-L-proline

: 92954-83-1
<1-(β-mercapto-β,β-pentamethylenepropionic acid),2-O-ethyl-D-tyrosine,4-valine,8-citrulline>vasopressin

Guidance literature:: Multi-step reaction with 2 steps

1: further educts: Boc-Val-OH, Boc-Phe-OH, Boc-D-Tyr(Et)-OH, p-nitrophenyl β-(benzylthio)-β,β-pentamethylenepropionate; solid phase method

2: 1.) sodium, 2.) potassium ferricyanide / 1.) liquid ammonia, reflux, 2.) water, pH=7, 20 min

With sodium; potassium hexacyanoferrate(III);
DOI:10.1021/jm00122a016

Reference yield:

: 4587-33-1
N-(tert-butyloxycarbonyl)-L-asparagine p-nitrophenyl ester

: 92954-83-1
<1-(β-mercapto-β,β-pentamethylenepropionic acid),2-O-ethyl-D-tyrosine,4-valine,8-citrulline>vasopressin

Guidance literature:: Multi-step reaction with 2 steps

1: further educts: Boc-Val-OH, Boc-Phe-OH, Boc-D-Tyr(Et)-OH, p-nitrophenyl β-(benzylthio)-β,β-pentamethylenepropionate; solid phase method

2: 1.) sodium, 2.) potassium ferricyanide / 1.) liquid ammonia, reflux, 2.) water, pH=7, 20 min

With sodium; potassium hexacyanoferrate(III);
DOI:10.1021/jm00122a016