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570-08-1

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570-08-1 Usage

Chemical Properties

Colorless liquid

Uses

Diethyl acetylmalonate is used as pharmaceutical intermediates.

Check Digit Verification of cas no

The CAS Registry Mumber 570-08-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 570-08:
(5*5)+(4*7)+(3*0)+(2*0)+(1*8)=61
61 % 10 = 1
So 570-08-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O5/c1-3-5(4-2)7(10)6(8(11)12)9(13)14/h5-6H,3-4H2,1-2H3,(H,11,12)(H,13,14)/p-2

570-08-1 Well-known Company Product Price

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  • Alfa Aesar

  • (L12482)  Diethyl acetylmalonate, tech. 85%   

  • 570-08-1

  • 2g

  • 323.0CNY

  • Detail
  • Alfa Aesar

  • (L12482)  Diethyl acetylmalonate, tech. 85%   

  • 570-08-1

  • 10g

  • 1155.0CNY

  • Detail

570-08-1SDS

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 Diethyl 2-acetylmalonate

1.2 Other means of identification

Product number -
Other names diethyl 2-acetylpropanedioate

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:570-08-1 SDS

570-08-1Relevant articles and documents

Schmidt,Schwochau

, p. 4491 (1967)

1,5,7-TRISUBSTITUTED ISOQUINOLINE DERIVATIVES, PREPARATION THEREOF, AND USE THEREOF IN MEDICINES

-

Paragraph 0150; 0217-0218, (2020/08/30)

The present disclosure relates to 1,5,7-trisubstituted isoquinoline derivatives, their preparation and pharmaceutical use. In particular, the present disclosure discloses a compound of formula (I) or a pharmaceutically acceptable salt, stereoisomer, solvate or prodrug thereof, and a preparation method and use thereof. The definitions of the groups in the formula can be found in the specification and claims.

Synthesis of β-arylacyl / β-heteroarylacyl-β-alkylidene malonates and their application in substituted pyridone synthesis

Wagh, Manoj Balu,Shankar,Mini,Krishnamohan,Madhubabu,Pal, Abir K.,Jayaprakash, Sarva,Krishna,Dahanukar, Vilas,Kumar, U. K. Syam,Gill

, p. 49 - 55 (2013/04/23)

A novel approach has been developed for the synthesis of β-arylacyl/β-heteroarylacyl-β-alkylidine malonates in moderate to good yields by the reaction of Stork aryl and heteroaryl enamine with β-chloroalkylidene malonates. The reaction involves conjugate

Synthesis of novel 5-alkyl/aryl/heteroaryl substituted diethyl 3,4-dihydro-2H-pyrrole-4,4-dicarboxylates by aziridine ring expansion of 2-[(aziridin-1-yl)-1-alkyl/aryl/heteroaryl-methylene]malonic acid diethyl esters

More, Satish S.,Mohan, T. Krishna,Kumar, Y. Sateesh,Kumar, U.K. Syam,Patel, Navin B.

scheme or table, p. 831 - 838 (2011/08/10)

A novel synthetic methodology has been developed for the synthesis of diethyl 5-alkyl/aryl/heteroaryl substituted 3,4-dihydro-2H-pyrrole-4,4- dicarboxylates (also called 2-substituted pyrroline-4,5-dihydro-3,3-dicarboxylic acid diethyl esters) by iodide i

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