36749-13-0

Basic information

• Product Name: 3-Ethoxypentane
• Synonyms: 3-Ethoxypentane
• CAS NO: 36749-13-0
• Molecular Formula: C7H16O
• Molecular Weight: 116.2013
• Mol File: 36749-13-0.mol
• Article Data: 5

Chemical Properties

• Melting Point: -95.35°C (estimate)
• Boiling Point: 117.3°C (estimate)
• Flash Point: 9°C
• Appearance: /
• Density: 0.7684 (estimate)
• Vapor Pressure: 29.6mmHg at 25°C
• Refractive Index: 1.3897 (estimate)
• CAS DataBase Reference: 3-Ethoxypentane(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Ethoxypentane(36749-13-0)
• EPA Substance Registry System: 3-Ethoxypentane(36749-13-0)

Safety Data

• Hazardous Substances Data: 36749-13-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H16O/c1-4-7(5-2)8-6-3/h7H,4-6H2,1-3H3

Upstream product

• 36749-09-4 3,3-diethoxypentane 
• 64-17-5 ethanol 
• 96-22-0 pentan-3-one 
• 4744-08-5 1,1-diethoxypropane 
• 97-93-8 triethylaluminum 
• 5670-78-0 ethyl diphenylmethyl ether 
• 925-90-6 ethylmagnesium bromide 
• 25801-57-4 ethyldiphenylorthoformate 
• 584-02-1 2-pentanol 
• 75-03-6 ethyl iodide 
• 616-24-0 3-aminopentane 

Relevant articles and documents

The Mechanism of Ethylene Elimination from the Oxonium Ions CH3CH2CH=O+CH2CH3 and (CH3)2C=O+CH2CH3

The reactions of the metastable oxonium ions CH3CH2CH=O+CH2CH3 and (CH3)2C=O+CH2CH3 are reported and discussed.Various mechanisms for ethylene elimination, which is the principal dissociation route for these ions, are considered.It is shown by means of 2H-labelling experiments and analysis of collision-induced dissociation spectra that routes involving ion-neutral complexes pre-empt 'conventional' mechanisms for these processes.In contrast, the behaviour of the lower homologues CH3CH2CH=OR+ and (CH3)2C=OR+ (R = H, CH3) is consistent with the operation of 'conventional' mechanisms for ethylene expulsion.This contrast is interpreted in energetic terms.The significance of these results for the chemistry of homologous and analogous 'onium' ions containing a Z+-R function (Z = O, S, NH, NCH3; R= CnH2n+1, n 2) is explained.

Nucleophilic Displacement with Heterocycles as Leaving Groups. Part 16. Reactions of Secondary Alkyl Primary Amines with 5,6,8,9-Tetrahydro-7-phenyldibenzoxanthylium Trifluoromethanesulphonate to give Intermediates Solvolysing without Rearrangement

Representative secondary alkyl primary amines R1R2CHNH2 react with the title pyrylium cation in acetic acid, alcohols, phenols, and NN-dimethylaniline acting as nucleophilic solvents to give O- and C-(secondary alkyl) products.Absence of carbenium ion rearrangements is consistent with reaction via intimate ion-molecule pairs formed rapidly from the corresponding pyridinium cations.

ACTION D'ORGANOMETALLIQUES SUR L'ORTHOFORMIATE DE DIPHENYLE ET D'ETHYLE. PREPARATION D'ACETALS MIXTES DE TYPE RCH(OC2H5)OC6H5

The reaction between an organometallic compound RM and the mixed orthoester (C6H5O)2CHOC2H5 gives either a mixed acetal RCH(OC2H5)OC6H5 or an ether R2CHOC2H5, depending on the structure of the organometallic compound used.