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163000-36-0

4-Heptenal, 6-oxo-, (4E)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 163000-36-0 Structure

  • Basic information

    1. Product Name: 4-Heptenal, 6-oxo-, (4E)- (9CI)
    2. Synonyms: 4-Heptenal, 6-oxo-, (4E)- (9CI)
    3. CAS NO:163000-36-0
    4. Molecular Formula: C7H10O2
    5. Molecular Weight: 126.1531
    6. EINECS: N/A
    7. Product Categories: ACETYLGROUP
    8. Mol File: 163000-36-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-Heptenal, 6-oxo-, (4E)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Heptenal, 6-oxo-, (4E)- (9CI)(163000-36-0)
    11. EPA Substance Registry System: 4-Heptenal, 6-oxo-, (4E)- (9CI)(163000-36-0)

  • 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: 163000-36-0(Hazardous Substances Data)

163000-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 163000-36-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,0,0 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 163000-36:
(8*1)+(7*6)+(6*3)+(5*0)+(4*0)+(3*0)+(2*3)+(1*6)=80
80 % 10 = 0
So 163000-36-0 is a valid CAS Registry Number.

163000-36-0Downstream Products

163000-36-0Relevant articles and documents

Ring-expansion protocol: Preparation of synthetically versatile dihydrotropones

Do, Young-Sun,Sun, Ruiying,Kim, Hee Jin,Yeo, Jung Eun,Bae, Sung-Hee,Koo, Sangho

body text, p. 917 - 920 (2009/06/20)

A ring-expansion protocol that consisted of the 1,2-addition of various enolate nucleophiles to 6-trimethylsiloxy-2- cyclohexene-1-one (1) and the NaIO4-promoted oxidative ring opening of the resulting diols 2, followed by an intramolecular Kno

The intramolecular Baylis-Hillman reaction: Easy preparation of versatile substrates, facile reactions, and synthetic applications

Yeo, Jung Eun,Yang, Xiuling,Kim, Hee Jin,Koo, Sangho

, p. 236 - 237 (2007/10/03)

We have developed a general and highly efficient method for the preparation of diverse ω-formyl-aα,β-unsaturated carbonyl compounds and optimized the conditions for the intramolecular Baylis-Hillman reactions of these compounds to provide various biologic

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