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147124-36-5

DIMETHYL 2-(2-CHLORO-6-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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  • 147124-36-5 Structure

  • Basic information

    1. Product Name: DIMETHYL 2-(2-CHLORO-6-NITROPHENYL)MALONATE
    2. Synonyms: DIMETHYL 2-(2-CHLORO-6-NITROPHENYL)MALONATE
    3. CAS NO:147124-36-5
    4. Molecular Formula: C11H10ClNO6
    5. Molecular Weight: 287.65
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 147124-36-5.mol

  • Chemical Properties

    1. Melting Point: 132-134°
    2. Boiling Point: 379.6±37.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.415±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 9.07±0.46(Predicted)
    10. CAS DataBase Reference: DIMETHYL 2-(2-CHLORO-6-NITROPHENYL)MALONATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: DIMETHYL 2-(2-CHLORO-6-NITROPHENYL)MALONATE(147124-36-5)
    12. EPA Substance Registry System: DIMETHYL 2-(2-CHLORO-6-NITROPHENYL)MALONATE(147124-36-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 147124-36-5(Hazardous Substances Data)

147124-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147124-36-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,1,2 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 147124-36:
(8*1)+(7*4)+(6*7)+(5*1)+(4*2)+(3*4)+(2*3)+(1*6)=115
115 % 10 = 5
So 147124-36-5 is a valid CAS Registry Number.

147124-36-5Relevant articles and documents

SPIROINDOLINONES AS DDR1 INHIBITORS

-

Page/Page column 65, (2017/09/07)

The present invention relates to compounds of formula (I): or pharmaceutically acceptable salts thereof, as well as processes for their manufacture, pharmaceutical compositions comprising them, and their use as medicaments.

A general oxindole synthesis

Quallich,Morrissey

, p. 51 - 53 (2007/10/02)

A general synthesis of indol-2(3H)-ones (oxindoles), was developed based on the addition of dimethyl malonate to commercially available halonitrobenzenes. The advantage of this route over many other oxindole syntheses was the regiochemical control of the substitution pattern on the aromatic ring.

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