What is the HEXANOIC ANHYDRIDE?

HEXANOIC ANHYDRIDE is clear colorless to light yellow liquid, while it's Molecular Formula is C12H22O3. clear colorless to light yellow liquid Hexanoic Anhydride, is used as a reactant in the total synthesis of acremomannolipin A via steroselective ß-mannosylation of 4,6,-O-benzylidene-protected mannosyl sulfoxide with a D-mannitol derivative.

What is the CAS number for HEXANOIC ANHYDRIDE?

The CAS number of HEXANOIC ANHYDRIDE is 2051-49-2.

What is HEXANOIC ANHYDRIDE (2051-49-2) used for?

HEXANOIC ANHYDRIDE, also known as caproic anhydride, is a colorless to light yellow liquid with chemical properties that make it a versatile compound in various industries. It is commonly used as a reactant in the synthesis of different organic compounds and has applications in pharmaceuticals, materials science, and more.InChI:InChI=1/C12H22O3/c1-3-5-7-9-11(13)15-12(14)10-8-6-4-2/h3-10H2,1-2H3

What is the HEXANOIC ANHYDRIDE?

HEXANOIC ANHYDRIDE is clear colorless to light yellow liquid, while it's Molecular Formula is C12H22O3. clear colorless to light yellow liquid Hexanoic Anhydride, is used as a reactant in the total synthesis of acremomannolipin A via steroselective β-mannosylation of 4,6,-O-benzylidene-protected mannosyl sulfoxide with a D-mannitol derivative.

What is the CAS number for HEXANOIC ANHYDRIDE?

The CAS number of HEXANOIC ANHYDRIDE is 2051-49-2.

What is HEXANOIC ANHYDRIDE (2051-49-2) used for?

HEXANOIC ANHYDRIDE, also known as caproic anhydride, is a colorless to light yellow liquid with chemical properties that make it a versatile compound in various industries. It is commonly used as a reactant in the synthesis of different organic compounds and has applications in pharmaceuticals, materials science, and more.InChI:InChI=1/C12H22O3/c1-3-5-7-9-11(13)15-12(14)10-8-6-4-2/h3-10H2,1-2H3

Factory Sells Best Quality HEXANOIC ANHYDRIDE 2051-49-2 with stock

Organic Chemicals

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HEXANOIC ANHYDRIDE

CAS No.: 2051-49-2
Purity: 99%

Factory Sells Best Quality HEXANOIC ANHYDRIDE 2051-49-2 with stock

Molecular Formula: C12H22O3
Molecular Weight: 214.305
Appearance/Colour: clear colorless to light yellow liquid
Vapor Pressure: 0.0263mmHg at 25°C
Melting Point: -40 °C
Refractive Index: n20/D 1.428(lit.)
Boiling Point: 246.999 °C at 760 mmHg
Flash Point: 116.614 °C
PSA： 43.37000
Density: 0.943 g/cm³
LogP: 3.21680

HEXANOIC ANHYDRIDE(Cas 2051-49-2) Usage

Preparation

To an ice-cooled flask containing 116 gm (1.0 mole) of n-caproic acid is added 21.0-23.10 gm (0.5-0.55 mole) of ketene at a rate of 0.45 mole/hr. The reaction mixture is fractionally distilled at atmospheric pressure to afford a forecut of acetone, acetic acid, and acetic anhydride. The oil bath is raised to 220°C over a 1-hr period, kept there for 3 hr to ensure complete removal of acetic acid, and then cooled. The distillation is continued under reduced pressure to afford 86-95 gm (80-87%), b.p. 109- 112°C (3 mm Hg) and b.p. 118-121°C (6 mm Hg).

Flammability and Explosibility

Notclassified

InChI:InChI=1/C12H22O3/c1-3-5-7-9-11(13)15-12(14)10-8-6-4-2/h3-10H2,1-2H3

2051-49-2 Relevant articles

A Semisynthetic Approach to New Immunoadjuvant Candidates: Site-Selective Chemical Manipulation of Escherichia coli Monophosphoryl Lipid A

D'Alonzo, Daniele,Cipolletti, Manuela,Tarantino, Giulia,Ziaco, Marcello,Pieretti, Giuseppina,Iadonisi, Alfonso,Palumbo, Giovanni,Alfano, Alberto,Giuliano, Mariateresa,De Rosa, Mario,Schiraldi, Chiara,Cammarota, Marcella,Parrilli, Michelangelo,Bedini, Emiliano,Corsaro, Maria M.

, p. 11053 - 11063 (2016)

A semisynthetic approach to novel lipid ...

Ketonization of hexanoic acid to diesel-blendable 6-undecanone on the stable zirconia aerogel catalyst

Lee, Yunsu,Choi, Jae-Wook,Suh, Dong Jin,Ha, Jeong-Myeong,Lee, Chang-Ha

, p. 288 - 293 (2015)

The ketonization of hexanoic acid, which...

One-pot electrochemical synthesis of acid anhydrides from alcohols

Kashparova,Papina,Kashparov,Zhukova, I. Yu.,Ilchibaeva,Kagan, E. Sh.

, p. 2733 - 2735 (2017/12/26)

One-pot indirect electrochemical oxidati...

Zinc(0)/dimethylformamide-mediated synthesis of symmetrical carboxylic anhydrides from acid chlorides

Serieys, Audrey,Botuha, Candice,Chemla, Fabrice,Ferreira, Franck,Pérez-Luna, Alejandro

, p. 5322 - 5323 (2008/12/22)

The high yielding synthesis of symmetric...

2051-49-2 Process route

: 450408-65-8
4,5-dichloro-2-hexanoyl-2H -pyridazin-3-one

: 932-22-9
4,5-dichloro-2H-pyridazin-3-one

: 2051-49-2
n-hexanoic anhydride

Conditions

Conditions	Yield
With zinc(II) chloride; In acetonitrile; for 6h; Heating;	91%

: 111-27-3
hexan-1-ol

: 6378-65-0
n-hexyl caproate

: 2051-49-2
n-hexanoic anhydride

: 66-25-1
hexanal

Conditions

Conditions	Yield
With 2,6-dimethylpyridine; 4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy; sodium hydrogencarbonate; potassium iodide; In dichloromethane; water; pH=8.6; Electrolysis;	25.5 %Chromat. 5.9 %Chromat. 66.1 %Chromat.