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CAS

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71127-36-1

diethyl methyl(2-nitrophenyl)malonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 71127-36-1 Structure

  • Basic information

    1. Product Name: diethyl methyl(2-nitrophenyl)malonate
    2. Synonyms: diethyl methyl(2-nitrophenyl)malonate
    3. CAS NO:71127-36-1
    4. Molecular Formula:
    5. Molecular Weight: 295.292
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 71127-36-1.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: diethyl methyl(2-nitrophenyl)malonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: diethyl methyl(2-nitrophenyl)malonate(71127-36-1)
    11. EPA Substance Registry System: diethyl methyl(2-nitrophenyl)malonate(71127-36-1)

  • 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: 71127-36-1(Hazardous Substances Data)

71127-36-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71127-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,1,2 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71127-36:
(7*7)+(6*1)+(5*1)+(4*2)+(3*7)+(2*3)+(1*6)=101
101 % 10 = 1
So 71127-36-1 is a valid CAS Registry Number.

71127-36-1Relevant articles and documents

Efficient synthesis of t-butyl 3-alkyl-N-hydroxy-oxindole-3-carboxylates from di-t-butyl 2-nitrophenylmalonates

Yamai, Yu-suke,Ishida, Kyoji,Natsutani, Itaru,Uesato, Shinichi,Nagaoka, Yasuo,Sumiyoshi, Takaaki

, p. 1257 - 1268 (2019/07/31)

– A selective and efficient synthesis of t-butyl 3-alkyl-N-hydroxy-oxindole-3-carboxylates from di-t-butyl 2-nitrophenylmalonates is described. A tandem reduction-cyclization approach involving reduction of di-t-butyl 2-methyl-(2-nitrophenyl)malonate to d

Nucleophilic aromatic substitution using Et3SiH/cat. t-Bu-P4 as a system for nucleophile activation

Ueno, Masahiro,Yonemoto, Misato,Hashimoto, Masahiro,Wheatley, Andrew E. H.,Naka, Hiroshi,Kondo, Yoshinori

, p. 2264 - 2266 (2008/01/03)

A novel type of deprotonative arylation of nucleophiles was conducted using Et3SiH/cat. t-Bu-P4 and the powerful SNAr reactions of aryl fluorides were accomplished using alcohols and malonates as nucleophiles. The Royal Society of Ch

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