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29149-74-4

ethyl 2-acetylhex-4-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 29149-74-4 Structure

  • Basic information

    1. Product Name: ethyl 2-acetylhex-4-enoate
    2. Synonyms:
    3. CAS NO:29149-74-4
    4. Molecular Formula: C10H16O3
    5. Molecular Weight: 184.2322
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 29149-74-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 234.3°C at 760 mmHg
    3. Flash Point: 93.7°C
    4. Appearance: N/A
    5. Density: 0.978g/cm3
    6. Vapor Pressure: 0.0533mmHg at 25°C
    7. Refractive Index: 1.446
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: ethyl 2-acetylhex-4-enoate(CAS DataBase Reference)
    11. NIST Chemistry Reference: ethyl 2-acetylhex-4-enoate(29149-74-4)
    12. EPA Substance Registry System: ethyl 2-acetylhex-4-enoate(29149-74-4)

  • 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: 29149-74-4(Hazardous Substances Data)

29149-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29149-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,4 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 29149-74:
(7*2)+(6*9)+(5*1)+(4*4)+(3*9)+(2*7)+(1*4)=134
134 % 10 = 4
So 29149-74-4 is a valid CAS Registry Number.

29149-74-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-acetylhex-4-enoate

1.2 Other means of identification

Product number -
Other names 2-Acetyl-hexen-(2)-saeureethylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:29149-74-4 SDS

29149-74-4Relevant articles and documents

Selenocyclofunctionalization of β-ketoamides: Synthesis of substituted dihydrofurans

Stefani, Hélio A.,Costa, Iguatemi M.,De O. Silva, Diogo,Menezes, Paulo H.,Rodrigues, Alessandro

, p. 141 - 152 (2007/10/03)

Selenocyclofunctionalization of α-substituted β-ketoamides obtained from the aminolysis of the ethyl acetoacetate yielded dihydrofurans in moderate to good yields.

Ruthenium complex-catalyzed allylic alkylation of carbonucleophiles with allylic carbonates

Zhang, Shi-Wei,Mitsudo, Take-aki,Kondo, Teruyuki,Watanabe, Yoshihisa

, p. 197 - 207 (2007/10/02)

Allylic carbonates except for allyl methyl carbonate reacted with carbonucleophiles such as ethyl acetoacetate in the presence of a catalytic amount of Ru(cod)(cot) in N-methylpiperidine at 80 deg C to give the corresponding monoallylated carbonucleophiles in high yields with high regioselectivity.The regioselectivity was quite different from that in the palladium-catalyzed reactions.The allylation of carbonucleophiles using allyl methyl carbonate selectively gave the diallylated carbonucleophiles in high yields.

SELECTIVE C-ALKYLATION OF 1,3-DICARBONYL COMPOUNDS

Antonioletti, Roberto,Bonadies, Francesco,Orelli, Liliana Raquel,Scettri, Arrigo

, p. 237 - 238 (2007/10/02)

Lithium hydroxide-mediated alkylation of 1,3-dicarbonyl compounds proves to proceed with high efficiency and selectivity.

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