2-Heptynoic acid

  • CAS:1483-67-6
  • purity:99%
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Details

Manufacturer supply high quality 2-Heptynoic acid 1483-67-6 with ISO standards

  • Molecular Formula: C7H10 O2
  • Molecular Weight: 126.155
  • Vapor Pressure: 0.0127mmHg at 25°C 
  • Melting Point: -3.32°C (estimate) 
  • Refractive Index: 1.4590-1.4620 
  • Boiling Point: 240.5°Cat760mmHg 
  • PKA: 2.67±0.10(Predicted) 
  • Flash Point: 113.5°C 
  • PSA: 37.30000 
  • Density: 1.033g/cm3 
  • LogP: 1.26460 

2-Heptynoic acid(Cas 1483-67-6) Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 78, p. 1221, 1956 DOI: 10.1021/ja01587a037

InChI:InChI=1/C7H10O2/c1-2-3-4-5-6-7(8)9/h2-4H2,1H3,(H,8,9)

1483-67-6 Relevant articles

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Khan,G.R. et al.

, p. 215 - 216 (1979)

-

-

Koehl,Wenzke

, p. 1418 (1937)

-

Cis -1,2-Bis(diphenylphosphino)ethylene copper(i) catalyzed C-H activation and carboxylation of terminal alkynes

Trivedi, Manoj,Smreker, Jacob R.,Singh, Gurmeet,Kumar, Abhinav,Rath, Nigam P.

, p. 14145 - 14151 (2017)

The reaction of cis-1,2-bis(diphenylphos...

-

Haynes,Jones

, p. 503,505 (1946)

-

A Schiff base-modified silver catalyst for efficient fixation of CO2 as carboxylic acid at ambient pressure

Wu, Zhilian,Sun, Lei,Liu, Qinggang,Yang, Xiaofeng,Ye, Xue,Hu, Yancheng,Huang, Yanqiang

, p. 2080 - 2085 (2017)

The fixation of CO2 as a carboxylic acid...

Microwave-assisted fabrication of a mixed-ligand [Cu4(μ3-OH)2]-cluster-based metal–organic framework with coordinatively unsaturated metal sites for carboxylation of terminal alkynes with carbon dioxide

Wang, Wen-Jing,Sun, Zhong-Hua,Chen, Sheng-Chun,Qian, Jun-Feng,He, Ming-Yang,Chen, Qun

, (2021/05/24)

The development of efficient and stable ...

Organocatalytic Strategy for the Fixation of CO2via Carboxylation of Terminal Alkynes

Shi, Jun-Bin,Bu, Qingqing,Liu, Bin-Yuan,Dai, Bin,Liu, Ning

, p. 1850 - 1860 (2021/01/14)

An organocatalytic strategy for the dire...

Method for rapidly preparing acetylenic acid and derivatives thereof based on microchannel continuous flow technology

-

Paragraph 0027, (2021/05/19)

The invention discloses a method for rap...

Fixation of CO2 as a carboxylic acid precursor by microcrystalline cellulose (MCC) supported Ag NPs: A more efficient, sustainable, biodegradable and eco-friendly catalyst

Shah, Dharmesh J.,Sharma, Anuj S.,Shah, Akshara P.,Sharma, Vinay S.,Athar, Mohd,Soni, Jigar Y.

supporting information, p. 8669 - 8676 (2019/06/14)

Silver nanoparticles supported on microc...

1483-67-6 Process route

carbon dioxide
124-38-9,18923-20-1

carbon dioxide

hex-1-yne
693-02-7

hex-1-yne

hept-2-ynoic acid
1483-67-6

hept-2-ynoic acid

Conditions
Conditions Yield
With hydrogenchloride; C54H44Cu2N2P4S2; caesium carbonate; In N,N-dimethyl-formamide; at 25 ℃; for 12h; Inert atmosphere;
95%
With caesium carbonate; In dimethyl sulfoxide; at 60 ℃; for 24h; under 760.051 Torr; Green chemistry;
94%
With caesium carbonate; In N,N-dimethyl-formamide; at 24 ℃; for 20h;
92%
With 3-(1-mesityl-1H-imidazol-3-ium-3-yl)propane-1-sulfonate; caesium carbonate; potassium iodide; silver(l) oxide; In N,N-dimethyl-formamide; at 35 ℃; for 24h; under 750.075 Torr; Darkness;
92%
carbon dioxide; hex-1-yne; With caesium carbonate; In N,N-dimethyl-formamide; at 120 ℃; for 18h; under 1900.13 Torr;
With hydrogenchloride; water; In N,N-dimethyl-formamide; pH=1;
90%
With n-butyllithium; In tetrahydrofuran; hexane; at -78 - 0 ℃; for 1.25h; Inert atmosphere;
87%
With caesium carbonate; In dimethyl sulfoxide; at 50 ℃; for 16h; under 760.051 Torr; Sealed tube;
87%
carbon dioxide; hex-1-yne; With caesium carbonate; N,N,N,N,-tetramethylethylenediamine; copper(l) chloride; In N,N-dimethyl-formamide; at 20 ℃; for 24h; under 760.051 Torr;
With hydrogenchloride; In dichloromethane; water; pH=1; Product distribution / selectivity;
85%
With 1,3-bis(4-methylbenzyl)imidazol-2-ylidene silver(I) chloride; caesium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 16h; under 760.051 Torr; Schlenk technique;
79%
With {[Cu43-OH)2(atrz)2(SIP)2]?4H2O}n; caesium carbonate; In N,N-dimethyl-formamide; at 100 ℃; for 16h; under 2250.23 Torr; Autoclave;
71%
carbon dioxide; hex-1-yne; With caesium carbonate; silver(I) iodide; In N,N-dimethyl-formamide; at 50 ℃; for 12h; under 1500.15 Torr; Autoclave;
With hydrogenchloride; In water; Cooling;
65%
carbon dioxide; hex-1-yne; With C24H30N3(1+)*Cl4Fe; caesium carbonate; In N,N-dimethyl-formamide; at 70 ℃; for 20h; under 760.051 Torr;
With hydrogenchloride; water; In N,N-dimethyl-formamide; at 20 ℃;
58%
With 1-(6-acetylpyridin-2-yl)-3-propyl-1H-benzo[d]imidazol-3-ium iodide; In dimethyl sulfoxide; at 60 ℃; for 24h; under 760.051 Torr;
58%
Multistep reaction; (i) Cs, heptane, THF, (ii) /BRN= 1900390/;
Multistep reaction; (i) nBuLi, (ii) /BRN= 1900390/, (iii) aq. H2SO4;
Multistep reaction; (i) NaAlH4, H2, diglyme, (ii) /BRN= 1900390/;
hex-1-yne; With n-butyllithium; In tetrahydrofuran; at -78 - -30 ℃; for 1.5h; Inert atmosphere;
carbon dioxide; In tetrahydrofuran; at -78 - 25 ℃; for 1.5h; Inert atmosphere;
hex-1-yne; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 1h; Inert atmosphere; Schlenk technique;
carbon dioxide; In tetrahydrofuran; at 0 ℃; Inert atmosphere; Schlenk technique;
hex-1-yne; With n-butyllithium; In tetrahydrofuran; at -10 - 0 ℃; for 0.00416667h;
carbon dioxide; In tetrahydrofuran; at 10 - 20 ℃; for 3.05556E-05h;
ethyl hept-2-ynoate
16930-95-3

ethyl hept-2-ynoate

hept-2-ynoic acid
1483-67-6

hept-2-ynoic acid

Conditions
Conditions Yield
With water; sodium hydroxide; In ethanol; at 20 ℃; for 2.5h; Schlenk technique; Sealed tube; Inert atmosphere;
88%
With water; sodium hydroxide; In ethanol; at 20 ℃; for 2.5h; Inert atmosphere;
85%
With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride; In diethyl ether; water; for 120h; Yield given;
With water; sodium hydroxide; In ethanol; Inert atmosphere;

1483-67-6 Upstream products

  • 18621-55-1
    18621-55-1

    trideca-5,8-diyn-7-ol

  • 124-38-9
    124-38-9

    carbon dioxide

  • 17689-03-1
    17689-03-1

    1-hexynyllithium

  • 55944-49-5
    55944-49-5

    1,3-dilithiohex-1-yne

1483-67-6 Downstream products

  • 18937-78-5
    18937-78-5

    methyl 2-heptynoate

  • 16930-95-3
    16930-95-3

    ethyl hept-2-ynoate

  • 15719-64-9
    15719-64-9

    methylammonium carbonate

  • 693-02-7
    693-02-7

    hex-1-yne