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4-FORMYLPHENYL 2-FUROATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 75350-30-0 Structure
  • Basic information

    1. Product Name: 4-FORMYLPHENYL 2-FUROATE
    2. Synonyms: ART-CHEM-BB B014264;AKOS B014264;4-FORMYLPHENYL 2-FUROATE;(4-formylphenyl) furan-2-carboxylate;(4-methanoylphenyl) furan-2-carboxylate;2-furancarboxylic acid (4-formylphenyl) ester;A2437/0103278;CBDivE_001469
    3. CAS NO:75350-30-0
    4. Molecular Formula: C12H8O4
    5. Molecular Weight: 216.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 75350-30-0.mol
  • Chemical Properties

    1. Melting Point: 95 °C(Solv: ethanol (64-17-5))
    2. Boiling Point: 360.8±22.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.292±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-FORMYLPHENYL 2-FUROATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-FORMYLPHENYL 2-FUROATE(75350-30-0)
    11. EPA Substance Registry System: 4-FORMYLPHENYL 2-FUROATE(75350-30-0)
  • Safety Data

    1. Hazard Codes: Xi
    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: 75350-30-0(Hazardous Substances Data)

75350-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75350-30-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,5 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75350-30:
(7*7)+(6*5)+(5*3)+(4*5)+(3*0)+(2*3)+(1*0)=120
120 % 10 = 0
So 75350-30-0 is a valid CAS Registry Number.

75350-30-0Relevant articles and documents

Synthesis, characterization, biological activity and molecular docking studies of novel schiff bases derived from thiosemicarbazide: Biochemical and computational approach

Tokal?, Feyzi Sinan,Taslimi, Parham,Usanmaz, Hande,Karaman, Muhammet,?endil, K?v?lc?m

, (2021/01/05)

In this study, eight new Schiff base derivatives (2a-h) were synthesized and their inhibition activities against Acetylcholinesterase (AChE), Butyrylcholinesterase (BChE), α-Glucosidase and Lactoperoxidase (LPO) were investigated. Structures of the synthe

Synthesis of cholesteryl esters of heterocyclic analogs of cinnamic acid and hetaroyloxycinnamic acids by the Wittig reaction

Listvan,Listvan,Shekel'

, p. 1480 - 1483 (2007/10/03)

The reaction of cholesteryl triphenylphosphonioacetate chloride with heterocyclic aldehydes and hetaroyloxyarenecarbaldehydes in the presence of base gave the corresponding cholesteryl esters of substituted propenoic acids possessing liquid crystal proper

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