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Carbamic acid, [2-(2-cyanoethoxy)-1,1-bis[(2-cyanoethoxy)methyl]ethyl]-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

439142-70-8

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439142-70-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 439142-70-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,9,1,4 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 439142-70:
(8*4)+(7*3)+(6*9)+(5*1)+(4*4)+(3*2)+(2*7)+(1*0)=148
148 % 10 = 8
So 439142-70-8 is a valid CAS Registry Number.

439142-70-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(2-cyanoethoxy)-1,1-bis-(2-cyanoethoxymethyl)ethyl]carbamic acid benzyl ester

1.2 Other means of identification

Product number -
Other names benzyl (1,3-bis(2-cyanoethoxy)-2-((2-cyanoethoxy)methyl)propan-2-yl)carbamate

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:439142-70-8 SDS

439142-70-8Relevant academic research and scientific papers

A novel 1 → 3 C-branched isocyanate monomer for resin amplification - A pseudo PS-PEG high-loading resin

Lebreton, Sylvain,Newcombe, Nicholas,Bradley, Mark

, p. 2479 - 2482 (2002)

High loading resins (up to 120 nmoles/bead) were preprared by solid-phase dendrimerisation using a novel 1→3 C-branched isocyanate monomer.

Biomimetic ferrichrome: Structural motifs for switching between narrow- and broad-spectrum activities in P. putida and E. coli

Olshvang, Evgenia,Szebesczyk, Agnieszka,Kozlowski, Henryk,Hadar, Yitzhak,Gumienna-Kontecka, Elzbieta,Shanzer, Abraham

supporting information, p. 20850 - 20858 (2015/12/11)

A series of novel ferrichrome (FC) analogs was designed based on the X-ray structure of FC in the FhuA transporter of Escherichia coli. Two strategies were employed: the first strategy optimized the overall size and relative orientation of H-bonding inter

Enabling ScFvs as multi-drug carriers: A dendritic approach

Sun, Chengzao,Wirsching, Peter,Janda, Kim D.

, p. 1761 - 1768 (2007/10/03)

To enable scFvs as multi-drug carriers, we designed and synthesized dendritic linker molecules bearing up to nine chlorambucil residues at the branch ends. A maleimide group was used at the focal point of the dendron for easy linkage to the scFv. Original

Solid-phase construction: High efficiency dendrimer synthesis using AB3 isocyanate-type monomers

Lebreton, Sylvain,How, Siew-Eng,Buchholz, Monika,Yingyongnarongkul, Boon-Ek,Bradley, Mark

, p. 3945 - 3953 (2007/10/03)

Solid-phase synthesis is an ideal tool for reactions that require high concentrations and excess reagents and forcing chemical conditions. One such chemistry is that required for dendrimer construction. In this paper the synthesis of a series of symmetric

Syntheses of dendritic linkers containing chlorambucil residues for the preparation of antibody-multidrug immunoconjugates

Sun, Chengzao,Wirsching, Peter,Janda, Kim D.

, p. 2213 - 2215 (2007/10/03)

A novel dendritic molecule with nine chlorambucil (CBL) residues on the surface and a maleimide moiety at the core terminus was synthesized using a convergent synthetic methodology. This molecule is ready for attachment to single-chain Fv antibodies (scFv

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