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109745-89-3

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109745-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109745-89-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,7,4 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 109745-89:
(8*1)+(7*0)+(6*9)+(5*7)+(4*4)+(3*5)+(2*8)+(1*9)=153
153 % 10 = 3
So 109745-89-3 is a valid CAS Registry Number.

109745-89-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name <N-(Benzyloxycarbonyl)-N-methyl-L-valyl>-L-valine methyl ester

1.2 Other means of identification

Product number -
Other names CbzNMeVal-ValOMe

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:109745-89-3 SDS

109745-89-3Downstream Products

109745-89-3Relevant articles and documents

Oxybenzotriazole free peptide coupling reagents for N-methylated amino acids

Coste, Jacques,Frerot, Eric,Jouin, Patrick,Castro, Bertrand

, p. 1967 - 1970 (1991)

The main product of N-methylated amino acid coupling, when oxybenzotriazole is present in the reagent (BOP, PyBOP, HBPyU) or as an additive (DCC/HOBt), is the weakly reactive benzotriazolyl ester. On the other hand, the corresponding new halogenated reage

Coupling N-Methylated Amino Acids Using PyBroP and PyCloP Halogenophosphonium Salts: Mechanism and Fields of Application

Coste, Jacques,Frerot, Eric,Jouin, Patrick

, p. 2437 - 2446 (1994)

PyBroP (1) and PyCloP (2), two halotripyrrolidinophosphonium hexafluorophosphates, are peptidecoupling reagents highly efficient for coupling N-methylated amino esters, in contrast with PyBOP (3), the hydroxybenzotriazolyl analogue.These halogenophosphonium salts 1 and 2 are convenient (one-pot reactions) stable solids soluble in conventional solvents.Use of them gave an excellent peptide yield with essentially no epimerization.Activation with these reagents probably involves the formation of an (acyloxy)phosphonium, as shown in the case of 2,4,6-trimethylbenzoic acid activation.In the case of reagents 1 and 2, oxazolone and/or a symmetrical anhydride were intermediates which were rapidly aminolyzed.In contrast, the benzotriazolyl ester intermediate which was formed with PyBOP (3) was poorly reactive with N-methylated amino esters.PyBroP (1) and PyCloP (2) were less efficient in the coupling of some Boc-amino acids because of N-carboxyanhydride formation; this was particularly the case when Boc-Val-OH or Boc-MeVal-OH was coupled with MeVal-OMe.

Polymer-bound TBTU as a new solid-supported reagent for peptide synthesis

Chinchilla, Rafael,Dodsworth, David J.,Nájera, Carmen,Soriano, José M.

, p. 2463 - 2466 (2007/10/03)

A new polymer-supported TBTU (P-TBTU) has been prepared from polystyrene-bound 1-hydroxybenzotriazole (P-HOBT) and used efficiently as a solid-supported reagent for peptide-coupling reactions, and is even effective with wet solvents. The P-HOBT can be rec

2-Mercaptopyridone 1-oxide-based uronium salts: New peptide coupling reagents

Bailen, Miguel A.,Chinchilla, Rafael,Dodsworth, David J.,Najera, Carmen

, p. 8936 - 8939 (2007/10/03)

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