Tr-L-Glu-OBn>

Base Information

Chemical Name:Tr-L-Glu-OBn>
CAS No.:95014-77-0
Molecular Formula:C₇₄H₇₇N₅O₁₂S₂
Molecular Weight:1292.58
Hs Code.:

Tr-L-Glu-OBn<L-Cys(MOB)-L-Glu-OBn<L-Cys(MOB)-Gly-OBn>>

Synonyms:

Suppliers and Price of Tr-L-Glu-OBn>

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 0 raw suppliers

Chemical Property of Tr-L-Glu-OBn>

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Tr-L-Glu-OBn>

There total 9 articles about Tr-L-Glu-OBn> 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:

: 97507-38-5
(S)-2-[(R)-2-Amino-3-(4-methoxy-benzylsulfanyl)-propionylamino]-4-[(R)-1-(benzyloxycarbonylmethyl-carbamoyl)-2-(4-methoxy-benzylsulfanyl)-ethylcarbamoyl]-butyric acid benzyl ester

: 73488-68-3
Tr-L-Glu(OBzl)-OH

: 95014-77-0
Tr-L-Glu-OBn>

Guidance literature:: With dicyclohexyl-carbodiimide; In dichloromethane; at 0 ℃; for 1h; Yield given;

Reference yield:

: 97507-31-8
Boc-Cys(MBzl)-Gly-OBzl

: 95014-77-0
Tr-L-Glu-OBn>

Guidance literature:: Multi-step reaction with 6 steps

1: TFA, anisole / 0.67 h / Ambient temperature

2: DCC / CH₂Cl₂

3: TFA, anisole / 0.08 h / 0 °C

4: DCC / CH₂Cl₂ / 0.5 h / 0 °C

5: TFA, anisole / 1 h / Ambient temperature

6: DCC / CH₂Cl₂ / 1 h / 0 °C

With methoxybenzene; dicyclohexyl-carbodiimide; trifluoroacetic acid; In dichloromethane;

Reference yield:

: 18942-46-6,58290-35-0
N-(tert-butyloxycarbonyl)-S-(4-methoxybenzyl)cysteine

: 95014-77-0
Tr-L-Glu-OBn>

Guidance literature:: Multi-step reaction with 7 steps

1: DCC / CH₂Cl₂ / 1 h / 0 °C

2: TFA, anisole / 0.67 h / Ambient temperature

3: DCC / CH₂Cl₂

4: TFA, anisole / 0.08 h / 0 °C

5: DCC / CH₂Cl₂ / 0.5 h / 0 °C

6: TFA, anisole / 1 h / Ambient temperature

7: DCC / CH₂Cl₂ / 1 h / 0 °C

With methoxybenzene; dicyclohexyl-carbodiimide; trifluoroacetic acid; In dichloromethane;