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z/e-3-(4-hydroxyphenyl)-3-pentene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 731812-99-0 Structure
  • Basic information

    1. Product Name: z/e-3-(4-hydroxyphenyl)-3-pentene
    2. Synonyms: z/e-3-(4-hydroxyphenyl)-3-pentene
    3. CAS NO:731812-99-0
    4. Molecular Formula:
    5. Molecular Weight: 162.232
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 731812-99-0.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: z/e-3-(4-hydroxyphenyl)-3-pentene(CAS DataBase Reference)
    10. NIST Chemistry Reference: z/e-3-(4-hydroxyphenyl)-3-pentene(731812-99-0)
    11. EPA Substance Registry System: z/e-3-(4-hydroxyphenyl)-3-pentene(731812-99-0)
  • 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: 731812-99-0(Hazardous Substances Data)

731812-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 731812-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,1,8,1 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 731812-99:
(8*7)+(7*3)+(6*1)+(5*8)+(4*1)+(3*2)+(2*9)+(1*9)=160
160 % 10 = 0
So 731812-99-0 is a valid CAS Registry Number.

731812-99-0Upstream product

731812-99-0Relevant articles and documents

Bioinspired Metal-Free Formal Decarbonylation of α-Branched Aliphatic Aldehydes at Ambient Temperature

Richter, Sven C.,Oestreich, Martin

, p. 8508 - 8512 (2019)

A sequence of a Baeyer–Villiger oxidation and a Lewis acid-promoted reduction of the resulting formate with Et3SiH enabled the metal-free formal decarbonylation of tertiary and secondary aliphatic aldehydes. The new methodology mimics the biosynthetic decarbonylation pathway through oxidative C?C bond cleavage rather than the C(O)?H bond activation known from conventional Tsuji–Wilkinson-type reactions. The substrate scope is complementary to existing transition-metal-catalyzed protocols.

VITAMIN D RECEPTOR MODULATORS

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Page/Page column 99-100, (2010/02/11)

The present invention relates to novel, non-secosteroidal, sulfonate and sulfonamide functional diaryl compounds with vitamin D receptor (VDR) modulating activity that are less hypercalcemic than 1α,25 dihydroxy vitamin D3. These compounds are useful for treating bone disease and psoriasis. X-15439

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