What is the 7-Bromoheptanenitrile?

7-Bromoheptanenitrile is clear yellow to yellow-brown liquid, while it's Molecular Formula is C7H12BrN. clear yellow to yellow-brown liquid 7-Bromoheptanenitrile was used in the synthesis of (±)-15-deoxyspergualin, a new immunosuppressive agent.

What is the CAS number for 7-Bromoheptanenitrile?

The CAS number of 7-Bromoheptanenitrile is 20965-27-9.

What is 7-Bromoheptanenitrile (20965-27-9) used for?

7-Bromoheptanenitrile is an organic compound that serves as an important intermediate in the synthesis of various pharmaceuticals and chemicals. It is characterized by its unique molecular structure, which includes a bromo and a nitrile functional group attached to a heptane chain.InChI:InChI=1/C7H12BrN/c8-6-4-2-1-3-5-7-9/h1-6H2

What is the 7-Bromoheptanenitrile?

7-Bromoheptanenitrile is clear yellow to yellow-brown liquid, while it's Molecular Formula is C7H12BrN. clear yellow to yellow-brown liquid 7-Bromoheptanenitrile was used in the synthesis of (±)-15-deoxyspergualin, a new immunosuppressive agent.

What is the CAS number for 7-Bromoheptanenitrile?

The CAS number of 7-Bromoheptanenitrile is 20965-27-9.

What is 7-Bromoheptanenitrile (20965-27-9) used for?

7-Bromoheptanenitrile is an organic compound that serves as an important intermediate in the synthesis of various pharmaceuticals and chemicals. It is characterized by its unique molecular structure, which includes a bromo and a nitrile functional group attached to a heptane chain.InChI:InChI=1/C7H12BrN/c8-6-4-2-1-3-5-7-9/h1-6H2

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7-Bromoheptanenitrile

CAS：20965-27-9
purity：99%

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Manufacturer supply high quality 7-Bromoheptanenitrile 20965-27-9 with GMP standards

Molecular Formula: C7H12BrN
Molecular Weight: 190.083
Appearance/Colour: clear yellow to yellow-brown liquid
Vapor Pressure: 0.012mmHg at 25°C
Refractive Index: n20/D 1.475(lit.)
Boiling Point: 260.7 °C at 760 mmHg
Flash Point: 111.5 °C
PSA： 23.79000
Density: 1.262 g/cm³
LogP: 2.85538

7-Bromoheptanenitrile(Cas 20965-27-9) Usage

InChI:InChI=1/C7H12BrN/c8-6-4-2-1-3-5-7-9/h1-6H2

20965-27-9 Relevant articles

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Heine et al.

, p. 4514 (1953)

Process for preparing azelaic acid

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Paragraph 0096; 0097, (2021/02/19)

A process for preparing azelaic acid is ...

Rapid radiosynthesis of [11C] and [14C]azelaic, suberic, and sebacic acids for in vivo mechanistic studies of systemic acquired resistance in plants

Best, Marcel,Gifford, Andrew N.,Kim, Sung Won,Babst, Ben,Piel, Markus,Roesch, Frank,Fowler, Joanna S.

experimental part, p. 39 - 43 (2012/06/29)

A recent report that the aliphatic dicar...

Applications of surfactant-modified clays to synthetic organic chemistry

Ghiaci,Sedaghat,Kalbasi,Abbaspur

, p. 5529 - 5534 (2007/10/03)

Two triphase catalysts (SLL) have been d...

Orthocarbonsaeure-ester mit 2,4,10-Trioxaadamantanstruktur als Carboxylschutzgruppe; Verwendung zur Synthese von substituierten Carbonsaeuren mit Hilfe von Grignard-Reagenzien

Voss, Gundula,Gerlach, Hans

, p. 2294 - 2307 (2007/10/02)

The surprising stability of 2,4,10-triox...

20965-27-9 Process route

: 629-03-8
1 ,6-dibromohexane

: 143-33-9,25596-52-5
sodium cyanide

: 629-40-3
octanedinitrile

: 20965-27-9
7-bromo-heptanonitrile

Conditions

Conditions	Yield
With 1-butyl-1,4-diazabicyclo[2.2.2]octane-1-ium chloride; In water; toluene; at 90 ℃; for 24h;	50 % Chromat. 18 % Chromat.
With 1-cetyl-4-aza-1-azonia bicyclo[2.2.2]octane chloride; In chloroform; water; at 58 ℃; for 24h;	37 % Chromat. 39 % Chromat.