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94305-41-6

(Z)-methyl 2-methyl-3,5-diphenylpent-2-en-4-ynoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 94305-41-6 Structure

  • Basic information

    1. Product Name: (Z)-methyl 2-methyl-3,5-diphenylpent-2-en-4-ynoate
    2. Synonyms: (Z)-methyl 2-methyl-3,5-diphenylpent-2-en-4-ynoate
    3. CAS NO:94305-41-6
    4. Molecular Formula:
    5. Molecular Weight: 276.335
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 94305-41-6.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)-methyl 2-methyl-3,5-diphenylpent-2-en-4-ynoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-methyl 2-methyl-3,5-diphenylpent-2-en-4-ynoate(94305-41-6)
    11. EPA Substance Registry System: (Z)-methyl 2-methyl-3,5-diphenylpent-2-en-4-ynoate(94305-41-6)

  • 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: 94305-41-6(Hazardous Substances Data)

94305-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94305-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,3,0 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 94305-41:
(7*9)+(6*4)+(5*3)+(4*0)+(3*5)+(2*4)+(1*1)=126
126 % 10 = 6
So 94305-41-6 is a valid CAS Registry Number.

94305-41-6Downstream Products

94305-41-6Relevant articles and documents

Combining NHC-Cu and Bronsted base catalysis: Enantioselective allylic substitution/conjugate additions with alkynylaluminum reagents and stereospecific isomerization of the products to trisubstituted allenes

Dabrowski, Jennifer A.,Haeffner, Fredrik,Hoveyda, Amir H.

, p. 7694 - 7699 (2013)

All-catalytic route to trisubstituted allenes: The first examples of catalytic enantioselective allylic substitution reactions that involve alkyne-based nucleophiles and lead to products having tertiary stereogenic centers are followed by an exceptionally

Synthesis of isocoumarins and α-pyrones via electrophilic cyclization

Yao, Tuanli,Larock, Richard C.

, p. 5936 - 5942 (2007/10/03)

A variety of substituted isocoumarins and α-pyrones are readily prepared in excellent yields under very mild reaction conditions by the reaction of o-(1-alkynyl)benzoates and (Z)-2-alken-4-ynoates with ICl, I2, PhSeCl, p-O2NC6/

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