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1,3,3-Trimethoxypropene, a chemical compound with the formula C6H12O3, is an organic compound belonging to the acetal class. It is characterized by two distinct alkoxy (OR) groups directly attached to the same carbon atom. This substance is slightly soluble in water, readily soluble in organic solvents, and has a heavy, fruity, and floral taste or smell. Although it is not classified as a dangerous or hazardous substance and is considered low in toxicity, it may cause eye, skin, and respiratory tract irritation on direct contact or inhalation.

17576-35-1

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17576-35-1 Usage

Uses

Used in Organic Synthesis:
1,3,3-Trimethoxypropene is used as a key intermediate in the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable building block for the production of a wide range of chemical products.
Used in Flavor and Fragrance Industry:
1,3,3-Trimethoxypropene is used as a flavoring agent and fragrance ingredient due to its heavy, fruity, and floral taste or smell. It is incorporated into food products, beverages, and perfumes to enhance their sensory qualities.
Used in Pharmaceutical Industry:
1,3,3-Trimethoxypropene is used as a starting material or intermediate in the synthesis of various pharmaceutical compounds. Its versatility in organic synthesis allows for the development of new drugs and therapeutic agents.
Used in Chemical Research:
1,3,3-Trimethoxypropene is used as a research compound in academic and industrial laboratories. Its unique properties and reactivity make it an interesting subject for studying reaction mechanisms, exploring new synthetic routes, and developing novel applications in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 17576-35-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,7 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17576-35:
(7*1)+(6*7)+(5*5)+(4*7)+(3*6)+(2*3)+(1*5)=131
131 % 10 = 1
So 17576-35-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O3/c1-7-5-4-6(8-2)9-3/h4-6H,1-3H3

17576-35-1SDS

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 1,3,3-trimethoxyprop-1-ene

1.2 Other means of identification

Product number -
Other names Acrolein,3-methoxy-,dimethyl acetal (6CI,8CI)

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:17576-35-1 SDS

17576-35-1Relevant academic research and scientific papers

Claisen Orthoester Rearrangement in the Direct Preparation of Z-Isositsirikine and Z-Geissoschizine Derivatives Possessing the Right Oxidation State at C-17

Lounasmaa, Mauri,Hanhinen, Pirjo,Jokela, Reija

, p. 8623 - 8648 (1995)

The Claisen orthoester rearrangement utilizing allylic alcohol 1 (or 2) and trimethyl 3-methoxyorthopropionate 13a leads to Z-isositsirikine derivatives 21a-22a (or 23a-24a) possessing one RO-function at C-17.In the cases of trialkyl 3,3-dialkoxyorthopropionates , the intermediate ketene acetals 25a,b do not rearrange according to the Claisen mechanism to form compounds 26a,b and/or possessing two two RO-functions at C-17.Syntheses of the intermediate orthoesters, trimethyl 3-methoxyorthopropionate 13a, trimethyl 3,3-dimethoxyorthopropionate 14a, trimethyl trans-3-methoxyorthoacrylate 20c, and triethyl 3,3-diethoxyorthopropionate 14b are described.

SYNTHESIS OF 2-(2-ALKOXYETHYLIDENE)-1,3-DIOXOLANES BY USING THE 1,3-DIOXOLANE RING AS A DOUBLE BOND DIRECTING GROUP

Aben, R. W. M.,Scheeren, J. W.

, p. 3597 - 3598 (2007/10/02)

The title compounds could be synthesized from 2-chloro-acetal precursors having a dioxolan ring as acetal function so that the double bond is directed towards the dioxolan ring.

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