beta-(Hydroxymethoxy)tricarballylic acid gamma-lactone allyl ester

Base Information

Chemical Name:beta-(Hydroxymethoxy)tricarballylic acid gamma-lactone allyl ester
CAS No.:110333-20-5
Molecular Formula:C₁₀H₁₂O₇
Molecular Weight:244.201
Hs Code.:
DSSTox Substance ID:DTXSID70911598
Nikkaji Number:J91.122D

Synonyms:BRN 0234842;beta-(Hydroxymethoxy)tricarballylic acid gamma-lactone allyl ester;110333-20-5;Tricarballylic acid, beta-(hydroxymethoxy)-, gamma-lactone, allyl ester;DTXSID70911598;LS-156982;5-(Allyloxycarbonylmethyl)-4-oxo-1,3-dioxolane-5-acetic acid;(5-Oxo-4-{2-oxo-2-[(prop-2-en-1-yl)oxy]ethyl}-1,3-dioxolan-4-yl)acetic acid

Suppliers and Price of beta-(Hydroxymethoxy)tricarballylic acid gamma-lactone allyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of beta-(Hydroxymethoxy)tricarballylic acid gamma-lactone allyl ester

Chemical Property:

Vapor Pressure:7.61E-09mmHg at 25°C
Boiling Point:436.6°Cat760mmHg
Flash Point:172.7°C
Density:1.33g/cm³
XLogP3:-0.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:7
Exact Mass:244.05830272
Heavy Atom Count:17
Complexity:349

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CCOC(=O)CC1(C(=O)OCO1)CC(=O)O

Technology Process of beta-(Hydroxymethoxy)tricarballylic acid gamma-lactone allyl ester

There total 3 articles about beta-(Hydroxymethoxy)tricarballylic acid gamma-lactone allyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

: 4767-12-8
4,4-(5-oxo-1,3-dioxolane)diacetic acid anhydride

: 107-18-6
allyl alcohol

: 110333-20-5
2-<4-<(allyloxycarbonyl)methyl>-5-oxo-1,3-dioxolan-4-yl>acetic acid

Guidance literature:: Heating;
DOI:10.1016/0960-894X(96)00444-1

Reference yield:

: 144-16-1
5-oxo-1,3-dioxolan-4-ylidenedi(acetic acid)

: 110333-20-5
2-<4-<(allyloxycarbonyl)methyl>-5-oxo-1,3-dioxolan-4-yl>acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / acetic anhydride / 2 h / Heating

2: 5 h / Heating

With acetic anhydride;
DOI:10.1016/S0040-4020(97)00210-X

Reference yield:

: 77-92-9,906507-37-7
citric acid

: 110333-20-5
2-<4-<(allyloxycarbonyl)methyl>-5-oxo-1,3-dioxolan-4-yl>acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 50 percent / 4 h / 145 °C

2: 100 percent / acetic anhydride / 2 h / Heating

3: 5 h / Heating

With acetic anhydride;
DOI:10.1016/S0040-4020(97)00210-X