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5567-51-1

3,4-Heptadien-1-ol, also known as 3,4-heptadien-1-ol, is an organic compound with the molecular formula C7H12O. It is a colorless liquid with a strong, pungent odor. This unsaturated alcohol is characterized by the presence of a carbon-carbon double bond between the third and fourth carbon atoms, as well as a hydroxyl group attached to the first carbon atom. 3,4-Heptadien-1-ol is an important intermediate in the synthesis of various fragrances, flavors, and pharmaceuticals due to its unique chemical structure and reactivity. It is commonly used in the production of natural and synthetic grapefruit and orange flavors, as well as in the creation of other citrus-like scents. The compound is also found in trace amounts in some essential oils, such as lemongrass oil, and can be synthesized through various chemical reactions, including the reduction of 3,4-heptadienal or the hydroboration of 3,4-heptadiyne.

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  • 5567-51-1 Structure

  • Basic information

    1. Product Name: 3,4-heptadien-1-ol
    2. Synonyms: 3,4-heptadien-1-ol
    3. CAS NO:5567-51-1
    4. Molecular Formula:
    5. Molecular Weight: 112.172
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5567-51-1.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: 3,4-heptadien-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4-heptadien-1-ol(5567-51-1)
    11. EPA Substance Registry System: 3,4-heptadien-1-ol(5567-51-1)

  • 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: 5567-51-1(Hazardous Substances Data)

5567-51-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5567-51-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,6 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5567-51:
(6*5)+(5*5)+(4*6)+(3*7)+(2*5)+(1*1)=111
111 % 10 = 1
So 5567-51-1 is a valid CAS Registry Number.

5567-51-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-heptadien-1-ol

1.2 Other means of identification

Product number -
Other names 3,4-Heptadien-1-ol

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 -
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More Details:5567-51-1 SDS

5567-51-1Upstream product

5567-51-1Relevant articles and documents

A comparative study of the synthetic paths from 1-butyne to 2E,4Z-heptadien-1-ol

Mavrov, M. V.,Chrelashvili, Z. G.,Serebryakov, E. P.

, p. 737 - 741 (1993)

2E,4Z-Heptadien-1-ol (1), the key intermediate in the synthesis of the grapevine moth sex pheromone, was obtained from 1-butyne by a number of alternative procedures, including various variants of the stereocontrolled building of the conjugated E,Z-diene system (Cadiot-Chodkiewicz cross-coupling, alkyne-vinyl halide cross-coupling catalyzed by palladium complexes, anionotropic allylic rearrangement, partial cis- and trans-reduction of the triple bond).None of them could provide for configurational uniformity of 1.The most acceptable path to obtain 1 in multigram amounts appears to be that which proceeds via the conjugated diynol and enynol intermediates with subsequent catalytic cis-hydrogenation.

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