What is the 3-Octenoic acid?

3-Octenoic acid is , while it's Molecular Formula is C8H14 O2. 3-Octenoic acid is a fatty acid used as a synthetic building block, and is naturally found bioactive component in some plant extracts, such as Bryonopsis laciniosa fruit extract.

What is the CAS number for 3-Octenoic acid?

The CAS number of 3-Octenoic acid is 1577-19-1.

What is 3-Octenoic acid (1577-19-1) used for?

3-Octenoic acid, a white solid with an oily, fatty aroma and a medium strength odor of the fatty type, is a naturally occurring bioactive component found in some plant extracts, such as Bryonopsis laciniosa fruit extract. It is also utilized as a synthetic building block in various applications due to its unique chemical properties.

What is the 3-Octenoic acid?

3-Octenoic acid is , while it's Molecular Formula is C8H14 O2. 3-Octenoic acid is a fatty acid used as a synthetic building block, and is naturally found bioactive component in some plant extracts, such as Bryonopsis laciniosa fruit extract.

What is the CAS number for 3-Octenoic acid?

The CAS number of 3-Octenoic acid is 1577-19-1.

What is 3-Octenoic acid (1577-19-1) used for?

3-Octenoic acid, a white solid with an oily, fatty aroma and a medium strength odor of the fatty type, is a naturally occurring bioactive component found in some plant extracts, such as Bryonopsis laciniosa fruit extract. It is also utilized as a synthetic building block in various applications due to its unique chemical properties.

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Product classification

3-Octenoic acid

CAS：1577-19-1
purity：99%

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Details

Reliable factory customized supply 3-Octenoic acid 1577-19-1

Molecular Formula: C8H14 O2
Molecular Weight: 142.198
Melting Point: 1.7°C (estimate)
Refractive Index: 1.4420-1.4470
Boiling Point: 244°Cat760mmHg
Flash Point: 141.3°C
PSA： 37.30000
Density: 0.955g/cm³
LogP: 2.20750

1577-19-1 Relevant articles

Palladium-Catalyzed Low Pressure Carbonylation of Allylic Alcohols by Catalytic Anhydride Activation

Schelwies, Mathias,Paciello, Rocco,Pelzer, Ralf,Siegel, Wolfgang,Breuer, Michael

supporting information, p. 9263 - 9266 (2021/05/27)

A direct carbonylation of allylic alcoho...

Enantioselective Alkylamination of Unactivated Alkenes under Copper Catalysis

Bai, Zibo,Zhang, Heng,Wang, Hao,Yu, Hanrui,Chen, Gong,He, Gang

supporting information, p. 1195 - 1202 (2021/02/05)

An enantioselective addition reaction of...

PROCESS FOR THE PREPARATION OF UNSATURATED CARBOXYLIC ACIDS BY CARBONYLATION OF ALLYL ALCOHOLS AND THEIR ACYLATION PRODUCTS

-

Paragraph 0231-0232, (2020/03/01)

The present invention relates to a proce...

Iridium-Catalyzed γ-Selective Hydroboration of γ-Substituted Allylic Amides

Zhao, Hongliang,Gao, Qian,Zhang, Yajuan,Zhang, Panke,Xu, Senmiao

supporting information, p. 2861 - 2866 (2020/04/02)

Reported here for the first time is the ...

1577-19-1 Process route

: 4938-52-7
1-hepten-3-ol

: 201230-82-2
carbon monoxide

: 1577-19-1,5163-67-7,5169-51-7
cis-3-octenoic acid

: 5163-67-7
(E)-oct-3-enoic acid

Conditions

Conditions	Yield
With dmap; palladium diacetate; acetic anhydride; triethylamine; triphenylphosphine; at 60 ℃; for 24h; under 7500.75 Torr; Overall yield = 26 percent; Overall yield = 2.4 g; Autoclave; Inert atmosphere;	56 % de
With dmap; palladium diacetate; acetic anhydride; triethylamine; triphenylphosphine; at 60 ℃; for 24h; under 7500.75 Torr; Overall yield = 26 percent; Overall yield = 2.4 g; Inert atmosphere; Autoclave;	56 % de

: 141-82-2
malonic acid

: 66-25-1
hexanal

: 1470-50-4
oct-2-enoic acid

: 1577-19-1
2-hexen-1-yl acetate

Conditions

Conditions	Yield
With pyridine; at 90 ℃; for 10h; Product distribution; var. tertiary amines;
With pyridine; at 90 ℃; for 10h; Yield given. Yields of byproduct given;
With 2,6-dimethylpyridine; at 90 ℃; for 10h; Yield given. Yields of byproduct given;