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Propanoic acid, 3-chloro-3-oxo-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 69479-87-4 Structure
  • Basic information

    1. Product Name: Propanoic acid, 3-chloro-3-oxo-, phenylmethyl ester
    2. Synonyms:
    3. CAS NO:69479-87-4
    4. Molecular Formula: C10H9ClO3
    5. Molecular Weight: 212.633
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 69479-87-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Propanoic acid, 3-chloro-3-oxo-, phenylmethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Propanoic acid, 3-chloro-3-oxo-, phenylmethyl ester(69479-87-4)
    11. EPA Substance Registry System: Propanoic acid, 3-chloro-3-oxo-, phenylmethyl ester(69479-87-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 69479-87-4(Hazardous Substances Data)

69479-87-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69479-87-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,7 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69479-87:
(7*6)+(6*9)+(5*4)+(4*7)+(3*9)+(2*8)+(1*7)=194
194 % 10 = 4
So 69479-87-4 is a valid CAS Registry Number.

69479-87-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 3-chloro-3-oxopropanoate

1.2 Other means of identification

Product number -
Other names Propanoic acid,3-chloro-3-oxo-,phenylmethyl ester

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:69479-87-4 SDS

69479-87-4Relevant articles and documents

MALONIC ESTER DERIVATIVES OF HETEROARYLPIPERIDINES AND -PIPERAZINES AS FUNGICIDES

-

Page/Page column 64, (2015/03/16)

Malonic ester derivatives of the formula (I), in which the symbols A1, A2, Y R10, p, X, R2, G, Q, L2 and R1 are each as defined in the description, and salts, metal complexes and N-oxides of the compounds of the formula (I), and the use thereof for controlling phytopathogenic harmful fungi and processes for preparing compounds of the formula (I).

Photochemical and thermal [2 + 2] cycloaddition to generate the bicyclo[3.2.0]heptane core of bielschowskysin

Farcet, Jean-Baptiste,Himmelbauer, Martin,Mulzer, Johann

supporting information, p. 4379 - 4398 (2013/07/26)

A bicyclic core fragment of the marine diterpenoid bielschowskysin has been synthesized. First, a large library of precursors for a photochemical [2 + 2] cycloaddition was prepared and tested, but with limited success. In the end, a thermal [2 + 2] cycloaddition followed by appropriate regio-and stereocontrolled functionalization efficiently gave access to the desired bicyclo[3.2.0]heptane core. An optimized route to this remarkable molecular structure is presented. Copyright

Short and versatile route to a key intermediate for lactacystin synthesis.

Bulman Page, Philip C,Hamzah, A Sazali,Leach, David C,Allin, Steven M,Andrews, David M,Rassias, Gerasimos A

, p. 353 - 355 (2007/10/03)

[reaction: see text] A key intermediate 14 for the synthesis of lactacystin 1 has been constructed in four steps and 33% overall yield. The key steps involve cyclization of a suitably functionalized glutamic acid derivative and concomitant alkylation of the resulting beta,beta-diketoester system, C-acylation of the cyclic alpha-amidoketone 9, and decarboxylbenzylation of 12. Alkylation of a related beta,beta-diketoester 5 was additionally achieved with several electrophiles.

A short preparation of an advanced intermediate for lactacystin synthesis: The complete carbon skeleton of clasto-lactacystin dihydroxyacid

Page, Philip C. Bulman,Leach, David C.,Hayman, Colin M.,Hamzah, A. Sazali,Allin, Steven M.,McKee, Vickie

, p. 1025 - 1027 (2007/10/03)

An advanced intermediate 22 for lactacystin synthesis, containing the full carbon skeleton of the pyrrolidinone component, has been achieved in four steps from a protected glycine ester.

New trisubstituted cyclopentadienyl ligands: Synthesis, characterisation and catalytic properties of mono and dinuclear cobalt, rhodium, iron and ruthenium complexes

Costa, Mirco,Dalcanale, Enrico,Dias, Francisco Santos,Graiff, Claudia,Tiripicchio, Antonio,Bigliardi, Lorenzo

, p. 179 - 193 (2007/10/03)

The synthesis of a set of dialkyl 4-alkoxycarbonylcyclopenta-1,3-diene-1,2-diacetates (1a-e) is described. Their coordinating abilities as anions have been investigated in relation to the formation of new sandwich, half-sandwich and dinuclear complexes and their structural features. We report here the preparation and characterisation of some complexes such as a mononuclear half-sandwich cobalt(1,5-COD) complex which has shown to be a very efficient catalyst for the cyclocotrimerisation reaction of alkynes and nitriles to pyridines. Half-sandwich rhodiumdicarbonyl complexes containing trisubstituted cyclopentadienyl ligands with ester chains of different length have been employed successfully as catalysts for hydroformylation of styrene. Finally ligands 1a-e have been used for the synthesis of ferrocenes and dinuclear carbonyl complexes of iron and ruthenium. The structures of the complexes 1,5-cycloctadiene[1-methoxycarbonyl-3,4-di(methoxycarbonylmethylene) cyclopentadienyl]cobalt [Co(MDMCp)COD] (9), dicarbonyl[1-methoxycarbonyl-3,4-di(methoxycarbonylmethylene)cyclopentadienyl] rhodium [Rh(MDMCp)(CO)2] (2a) and of a new ferrocene complex [Fe(MDMCp)2] (15a) have been determined by X-ray diffraction methods.

The use of γ-turn mimetics to define peptide secondary structure

Callahan,Newlander,Burgess,Eggleston,Nichols,Wong,Huffman

, p. 3479 - 3488 (2007/10/02)

A novel γ-turn mimetic 2 has been prepared based on retro amide peptide design. Incorporation of this mimetic into linear peptide fibrinogen receptor antagonist 7 (GPIIb/IIIa receptor) affords the opportunity to test models of antagonist pharmacophore.

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