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Technology Process of S-(β-2,4,6-trimethylbenzyl)mercaptopropionyl-O-tert-butyl-L-tyrosyl-L-phenylalanyl-L-glutaminyl-L-asparaginyl-S-(2,4,6-trimethylbenzyl)-L-cysteinyl-L-prolyl-NG-p-toluenesulfonyl-L-arginyl-L-glycine amide

S-(β-2,4,6-trimethylbenzyl)mercaptopropionyl-O-tert-butyl-L-tyrosyl-L-phenylalanyl-L-glutaminyl-L-asparaginyl-S-(2,4,6-trimethylbenzyl)-L-cysteinyl-L-prolyl-NG-p-toluenesulfonyl-L-arginyl-L-glycine amide

Base Information
  • Chemical Name:S-(β-2,4,6-trimethylbenzyl)mercaptopropionyl-O-tert-butyl-L-tyrosyl-L-phenylalanyl-L-glutaminyl-L-asparaginyl-S-(2,4,6-trimethylbenzyl)-L-cysteinyl-L-prolyl-NG-p-toluenesulfonyl-L-arginyl-L-glycine amide
  • CAS No.:78221-84-8
  • Molecular Formula:C77H104N14O14S3
  • Molecular Weight:1545.96
  • Hs Code.:
S-(β-2,4,6-trimethylbenzyl)mercaptopropionyl-O-tert-butyl-L-tyrosyl-L-phenylalanyl-L-glutaminyl-L-asparaginyl-S-(2,4,6-trimethylbenzyl)-L-cysteinyl-L-prolyl-N<sup>G</sup>-p-toluenesulfonyl-L-arginyl-L-glycine amide

Synonyms:

Suppliers and Price of S-(β-2,4,6-trimethylbenzyl)mercaptopropionyl-O-tert-butyl-L-tyrosyl-L-phenylalanyl-L-glutaminyl-L-asparaginyl-S-(2,4,6-trimethylbenzyl)-L-cysteinyl-L-prolyl-NG-p-toluenesulfonyl-L-arginyl-L-glycine amide
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Chemical Property of S-(β-2,4,6-trimethylbenzyl)mercaptopropionyl-O-tert-butyl-L-tyrosyl-L-phenylalanyl-L-glutaminyl-L-asparaginyl-S-(2,4,6-trimethylbenzyl)-L-cysteinyl-L-prolyl-NG-p-toluenesulfonyl-L-arginyl-L-glycine amide
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Technology Process of S-(β-2,4,6-trimethylbenzyl)mercaptopropionyl-O-tert-butyl-L-tyrosyl-L-phenylalanyl-L-glutaminyl-L-asparaginyl-S-(2,4,6-trimethylbenzyl)-L-cysteinyl-L-prolyl-NG-p-toluenesulfonyl-L-arginyl-L-glycine amide

There total 1 articles about S-(β-2,4,6-trimethylbenzyl)mercaptopropionyl-O-tert-butyl-L-tyrosyl-L-phenylalanyl-L-glutaminyl-L-asparaginyl-S-(2,4,6-trimethylbenzyl)-L-cysteinyl-L-prolyl-NG-p-toluenesulfonyl-L-arginyl-L-glycine amide 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:

C<sub>64</sub>H<sub>88</sub>N<sub>14</sub>O<sub>13</sub>S<sub>2</sub>*ClH
78221-79-1

C64H88N14O13S2*ClH

p-nitrophenyl S-(β-2,4,6-trimethylbenzyl)mercaptopropionate
78221-83-7

p-nitrophenyl S-(β-2,4,6-trimethylbenzyl)mercaptopropionate

S-(β-2,4,6-trimethylbenzyl)mercaptopropionyl-O-tert-butyl-L-tyrosyl-L-phenylalanyl-L-glutaminyl-L-asparaginyl-S-(2,4,6-trimethylbenzyl)-L-cysteinyl-L-prolyl-N<sup>G</sup>-p-toluenesulfonyl-L-arginyl-L-glycine amide
78221-84-8

S-(β-2,4,6-trimethylbenzyl)mercaptopropionyl-O-tert-butyl-L-tyrosyl-L-phenylalanyl-L-glutaminyl-L-asparaginyl-S-(2,4,6-trimethylbenzyl)-L-cysteinyl-L-prolyl-NG-p-toluenesulfonyl-L-arginyl-L-glycine amide

Guidance literature:
With 1-ethyl-piperidine; In N,N-dimethyl-formamide; for 48h;
DOI:10.1135/cccc19810286
upstream raw materials:

C64H88N14O13S2*ClH

p-nitrophenyl S-(β-2,4,6-trimethylbenzyl)mercaptopropionate

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