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15110-17-5

DIETHYL (3,3-DIETHOXYPROPYL)PHOSPHONATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 15110-17-5 Structure

  • Basic information

    1. Product Name: DIETHYL (3,3-DIETHOXYPROPYL)PHOSPHONATE
    2. Synonyms: DIETHYL (3,3-DIETHOXYPROPYL)PHOSPHONATE;diethyl(3,3-diethoxypropyl)phosphonate95+%;Diethyl (3,3-diethoxypropyl)phosphonate, stabilized with max. 1% w/w Na2CO3, 95%;Diethyl(3,3-diethoxypropyl)phosphonate, stabilized, 98 %;Diethyl (3,3-diethoxypropyl)phosphonate,95%,stabilized with max. 1% w/w Na2CO3;Diethyl (2,2-diethoxypropyl)phosphonate;Diethyl (3,3-diethoxyprop-1-yl)phosphonate;3-(Diethoxyphosphoryl)propanaldehyde diethyl acetal
    3. CAS NO:15110-17-5
    4. Molecular Formula: C11H25O5P
    5. Molecular Weight: 268.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 15110-17-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 98-100 °C
    3. Flash Point: 170.2 °C
    4. Appearance: Clear light yellow to orange/Liquid
    5. Density: 1.031 g/cm3
    6. Vapor Pressure: 0.000239mmHg at 25°C
    7. Refractive Index: 1.429-1.432
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: DIETHYL (3,3-DIETHOXYPROPYL)PHOSPHONATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: DIETHYL (3,3-DIETHOXYPROPYL)PHOSPHONATE(15110-17-5)
    12. EPA Substance Registry System: DIETHYL (3,3-DIETHOXYPROPYL)PHOSPHONATE(15110-17-5)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 37/39-26-24/25
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 15110-17-5(Hazardous Substances Data)

15110-17-5 Usage

Chemical Properties

clear light yellow to orange liquid

Check Digit Verification of cas no

The CAS Registry Mumber 15110-17-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,1 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15110-17:
(7*1)+(6*5)+(5*1)+(4*1)+(3*0)+(2*1)+(1*7)=55
55 % 10 = 5
So 15110-17-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H25O5P/c1-5-13-11(14-6-2)9-10-17(12,15-7-3)16-8-4/h11H,5-10H2,1-4H3

15110-17-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Diethyl (3,3-diethoxypropyl)phosphonate

1.2 Other means of identification

Product number -
Other names 3-diethoxyphosphoryl-1,1-diethoxypropane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15110-17-5 SDS

15110-17-5Relevant articles and documents

SYNTHESIS OF SOME BIOLOGICALLY ACTIVE CYCLOPENTENONES USING NEW ORGANOPHOSPHORUS REAGENTS

Mikolajczyk, M.,Grzejszczak, S.,Midura, W.,Zatorski, A.

, p. 175 - 178 (2007/10/02)

The use of organic phosphorus and sulfur compounds in the general synthesis of biologically active functionalized cyclopentenones is presented.

PREPARATION ET CONVERSION D'ω-FORMYLALKYLPHOSPHONATES EN ACIDES AMINOCARBOXYALKYLPHOSPHONIQUES

Varlet, J. M.,Fabre, G.,Sauveur, F.,Collignon, N.,Savignac, Ph.

, p. 1377 - 1384 (2007/10/02)

ω-Formylalkylphosphonates by acid hydrolysis of the corresponding acetals obtained from triethylphosphite and bromoacetals has been described.In aqueous solution in the presence of cyanide and amines these compounds give aminonitriles (Strecker) or hydantoins (Bucherer).These reactions give access to a large variety of compounds which by acid hydrolysis (Strecker) or basic then acid hydrolysis (Bucherer) lead to pure aminocarboxalkylphosphonic acids (phosphonoalanine, etc.).

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