238413-45-1

Basic information

• Product Name: Oxiranecarboxylic acid, 3-cyclopropyl-, methyl ester, (2S,3R)- (9CI)
• Synonyms: Oxiranecarboxylic acid, 3-cyclopropyl-, methyl ester, (2S,3R)- (9CI)
• CAS NO: 238413-45-1
• Molecular Formula: C7H10O3
• Molecular Weight: 142.1525
• Product Categories: CARBOXYLICESTER
• Mol File: 238413-45-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Oxiranecarboxylic acid, 3-cyclopropyl-, methyl ester, (2S,3R)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Oxiranecarboxylic acid, 3-cyclopropyl-, methyl ester, (2S,3R)- (9CI)(238413-45-1)
• EPA Substance Registry System: Oxiranecarboxylic acid, 3-cyclopropyl-, methyl ester, (2S,3R)- (9CI)(238413-45-1)

Safety Data

• Hazardous Substances Data: 238413-45-1(Hazardous Substances Data)

Upstream product

• 96-34-4 methyl chloroacetate 
• 1489-69-6 Cyclopropanecarboxaldehyde 
• 178248-33-4 methyl (2S,3R)-3-cyclopropyl-2,3-dihydroxypropionate 
• 98272-33-4 methyl 3-cyclopropylacrylate 

Downstream Products

• 56105-19-2 2-cyclopropylacetaldehyde 
• 2566-44-1 1-cyclopropylethanol 

Relevant articles and documents

PROCESSES FOR PREPARATION OF CYCLOPROPYLETHANOL, CYCLO-PROPYLACETONITRILE AND INTERMEDIATES OF BOTH

A process for preparation of cyclopropylethanol, which comprises subjecting a 3-cyclopropyl-2,3-epoxypropionic acid ester to solvolysis, treating the product of the solvolysis with an acid to obtain cyclopropylacetaldehyde, and reducing the obtained cyclopropylacetaldehyde; and a process for preparation of cyclopropylacetonitrile, which comprises subjecting a 3-cyclopropyl-2,3-epoxypropionic acid ester to solvolysis in the presence of a base, treating the product of the solvolysis with an acid to obtain cyclopropylacetaldehyde, reacting the obtained cyclopropylacetaldehyde with hydroxylamine or salts thereof to obtain cyclopropaneacetaldehyde oxime, and reacting the obtained cyclopropaneacetaldehyde oxime with acetic anhydride. According to the present invention, cyclopropylethanol and cyclopropylacetonitrile can be prepared at low costs and industrially advantageously.

Baccatin derivatives and processes for preparing the same

A compound represented by the formula [I]: STR1 wherein R3 represents a lower alkanoyl group; R4 represents a substituted or unsubstituted benzoyl group; ring A represents a substituted or unsubstituted cyclopropane ring; X represent