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CAS

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306775-04-2

2-hept-6-en-1-ynyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 306775-04-2 Structure

  • Basic information

    1. Product Name: 2-hept-6-en-1-ynyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
    2. Synonyms: 2-hept-6-en-1-ynyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
    3. CAS NO:306775-04-2
    4. Molecular Formula:
    5. Molecular Weight: 220.12
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 306775-04-2.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: 2-hept-6-en-1-ynyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-hept-6-en-1-ynyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane(306775-04-2)
    11. EPA Substance Registry System: 2-hept-6-en-1-ynyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane(306775-04-2)

  • 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: 306775-04-2(Hazardous Substances Data)

306775-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 306775-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,6,7,7 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 306775-04:
(8*3)+(7*0)+(6*6)+(5*7)+(4*7)+(3*5)+(2*0)+(1*4)=142
142 % 10 = 2
So 306775-04-2 is a valid CAS Registry Number.

306775-04-2Downstream Products

306775-04-2Relevant articles and documents

Ruthenium-catalyzed enyne metathesis of acetylenic boronates: A concise route for the construction of cyclic 1,3-dienylboronic esters

Renaud, Johanne,Graf, Claus-Dieter,Oberer, Lukas

, p. 3101 - 3104 (2007/10/03)

The operationally simple and highly efficient metathesis of enynes bearing an acetylenic dioxaborolane moiety provides straightforward access to carbocyclic and heterocyclic 1,3-dienyl-2-boronates [Eq. (1)]. Dienes of this class readily undergo Diels-Alder cycloaddition reactions with high regio- and stereoselectivity.

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