4211-33-0

Basic information

• Product Name: (E) 3-Methyl-5-(2,2,6-trimethylcyclohexen-1-yl)-2-pentenoic Acid
• Synonyms: (E) 3-Methyl-5-(2,2,6-trimethylcyclohexen-1-yl)-2-pentenoic Acid
• CAS NO: 4211-33-0
• Molecular Weight: 236.354
• Mol File: 4211-33-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E) 3-Methyl-5-(2,2,6-trimethylcyclohexen-1-yl)-2-pentenoic Acid(CAS DataBase Reference)
• NIST Chemistry Reference: (E) 3-Methyl-5-(2,2,6-trimethylcyclohexen-1-yl)-2-pentenoic Acid(4211-33-0)
• EPA Substance Registry System: (E) 3-Methyl-5-(2,2,6-trimethylcyclohexen-1-yl)-2-pentenoic Acid(4211-33-0)

Safety Data

• Hazardous Substances Data: 4211-33-0(Hazardous Substances Data)

Upstream product

• 854725-70-5 3-hydroxy-3-methyl-5-(2,6,6-trimethyl-cyclohex-1-enyl)-valeric acid 
• 462-11-3 (2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrienoic acid 
• 41641-09-2 4-(1-Hydroxy-2,2,6-trimethylcyclohexyl)-3-butyn-2-ol 
• 82462-59-7 4-(1-Hydroxy-2,2,6-trimethylcyclohexyl)-2-butanol 
• 446293-91-0 4-(2,6,6-trimethyl-cyclohex-1-enyl)-butan-2-ol 
• 17283-81-7 4-(2,6,6-Trimethyl-cyclohex-1-enyl)-butan-2-on 
• 3675-00-1 methyl (E,E)-farnesoate 
• 236744-59-5 Ethyl 3-Methyl-5-(2,2,6-trimethylcyclohexen-1-yl)-2-pentenoate 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 71-43-2 benzene 

Downstream Products

• 468-70-2 Bicyclofarnesic acid 
• 170032-69-6 (E)-3-Methyl-5-(2,6,6-trimethyl-cyclohex-1-enyl)-pent-2-enoic acid (R)-1-acetoxymethyl-2-(4-methoxy-benzyloxy)-ethyl ester 
• 170032-68-5 (E)-3-Methyl-5-(2,6,6-trimethyl-cyclohex-1-enyl)-pent-2-enoic acid (R)-1-acetoxymethyl-2-(tert-butyl-dimethyl-silanyloxy)-ethyl ester 
• 170032-67-4 (E)-3-Methyl-5-(2,6,6-trimethyl-cyclohex-1-enyl)-pent-2-enoic acid (R)-2-(tert-butyl-dimethyl-silanyloxy)-1-(4-methoxy-benzyloxymethyl)-ethyl ester 
• 125254-79-7 β-Cyclofarnesylic acid chloride 
• 4179-00-4 Methyl (E)-3-methyl-5-(2,6,6-trimethylcyclohexen-1-yl)-2-pentenoate 
• 468-70-2 rac-drim-7-en-11-oic acid 
• 57023-47-9 3-methyl-5-(2,2,6-trimethyl-cyclohexyl)-valeric acid 

Relevant articles and documents

Isolation and synthesis of tanyolides A and B, metabolites of the nudibranch Sclerodoris tanya

The nudibranch Sclerodoris tanya, which was collected intertidally at La Jolla, contains two sesquiterpene glyceride esters, tanyolides A (4) and B (5). The structures of the tanyolides were elucidated by interpretation of spectral data. The absolute configuration of tanyolide B (5) was determined by synthesis of both enantiomers and the structure of tanyolide A (4) was also confirmed by synthesis. The tanyolides, which are located primarily in the dorsal mantle, deter feeding by two ecologically-relevant predatory fish.