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30094-28-1 Usage

Synthesis Reference(s)

Synthesis, p. 661, 1986 DOI: 10.1055/s-1986-31739

Check Digit Verification of cas no

The CAS Registry Mumber 30094-28-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,0,9 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30094-28:
81 % 10 = 1
So 30094-28-1 is a valid CAS Registry Number.



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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017


1.1 GHS Product identifier

Product name 2-diethoxyphosphorylpropanoic acid

1.2 Other means of identification

Product number -
Other names a-(Diethylphosphono)propionic acid

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:30094-28-1 SDS

30094-28-1Relevant articles and documents

Vinylogous Dehydration by a Polyketide Dehydratase Domain in Curacin Biosynthesis

Fiers, William D.,Dodge, Greg J.,Sherman, David H.,Smith, Janet L.,Aldrich, Courtney C.

, p. 16024 - 16036 (2016)

Polyketide synthase (PKS) enzymes continue to hold great promise as synthetic biology platforms for the production of novel therapeutic agents, biofuels, and commodity chemicals. Dehydratase (DH) catalytic domains play an important role during polyketide

Modular total synthesis of archazolid A and B

Menche, Dirk,Hassfeld, Jorma,Li, Jun,Mayer, Kerstin,Rudolph, Sven

supporting information; experimental part, p. 7220 - 7229 (2010/02/17)

(Chemical Equation Presented) A modular total synthesis of the potent V-ATPase inhibitors archazolid A and B is reported. The convergent preparation was accomplished by late-stage diversification of joint intermediates. Key synthetic steps involve asymmetric boron-mediated aldol reactions, two consecutive Still-Gennari olefinations to set the characteristic (Z,Z)-diene system, a Brown crotyboration, and a diastereo-selective aldol condensation of highly elaborate intermediates. For macrocyclization, both an HWE reaction and a Heck coupling were successfully employed to close the 24-membered macrolactone. During the synthetic campaign, a generally useful protocol for an E-selective Heck reaction of nonactivated alkenes and a method for the direct nucleophilic displacement of the Abiko-Masamune auxiliary with sterically hindered nucleophiles were developed. The expedient and flexible strategy will enable further SAR studies of the archazolids and more detailed evaluations of target-inhibitor interactions. 2009 American Chemical Society.

A facile Horner-Wadsworth-Emmons route to 2-quinolones

Peters, Jens-Uwe,Capuano, Tony,Weber, Silja,Kritter, Stéphane,S?gesser, Matthias

, p. 4029 - 4032 (2008/09/20)

2-Quinolones are prepared from o-aminophenylketones by N-acylation with phosphonoalkanoylchlorides, followed by an intramolecular Horner-Wadsworth-Emmons olefination. The transformation proceeds under mild conditions, is generally applicable, gives good yields and can be performed either in two steps or as a one-pot reaction.

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