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Cyclohexanol, 1,1'-(1,3-butadiyne-1,4-diyl)bis-, diacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 99413-16-8 Structure
  • Basic information

    1. Product Name: Cyclohexanol, 1,1'-(1,3-butadiyne-1,4-diyl)bis-, diacetate
    2. Synonyms:
    3. CAS NO:99413-16-8
    4. Molecular Formula: C20H26O4
    5. Molecular Weight: 330.424
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 99413-16-8.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: Cyclohexanol, 1,1'-(1,3-butadiyne-1,4-diyl)bis-, diacetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanol, 1,1'-(1,3-butadiyne-1,4-diyl)bis-, diacetate(99413-16-8)
    11. EPA Substance Registry System: Cyclohexanol, 1,1'-(1,3-butadiyne-1,4-diyl)bis-, diacetate(99413-16-8)
  • 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: 99413-16-8(Hazardous Substances Data)

99413-16-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99413-16-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,4,1 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 99413-16:
(7*9)+(6*9)+(5*4)+(4*1)+(3*3)+(2*1)+(1*6)=158
158 % 10 = 8
So 99413-16-8 is a valid CAS Registry Number.

99413-16-8Relevant articles and documents

Transition metal-free dimerization of alkynes using hypervalent iodine reagents

Sch?rgenhumer, Johannes,Waser, Mario

, p. 1678 - 1680 (2016)

This communication describes the use of hypervalent iodine reagents to facilitate the homo-coupling of terminal alkynes. A variety of different aliphatic and aromatic alkynes were successfully dimerized when using acetoxy-benziodoxole as the activating agent under operationally simple transition metal-free conditions.

A NEW METHOD FOR THE SYNTHESIS OF VINYL- AND DI-ALLENES ASSISTED BY ORGANOALUMINIUM CONPOUNDS

Tolstikov, G. A.,Romanova, T. Yu.,Kuchin, A. V.

, p. 71 - 82 (2007/10/02)

The interactions of organoaluminium reagents with acetates of substituted propargyl alcohols have been considered as the most appropriate method to synthesize allenes.Studies have been carried out on the synthesis of vinyl- and di-allenes, employing both

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