CAS No. 173485-79-5

1H-Indene-4-carboxaldehyde,7-(acetyloxy)-2,3,5,6,7,7a-hexahydro-3-(hydroxymethyl)-1,1,3,5-tetramethyl-,[3S-(3a,5a,7a,7aa)]-

Identification

Catalog number	1335195
Chemical name	1H-Indene-4-carboxaldehyde,7-(acetyloxy)-2,3,5,6,7,7a-hexahydro-3-(hydroxymethyl)-1,1,3,5-tetramethyl-,[3S-(3a,5a,7a,7aa)]-
CAS RN	173485-79-5
Molecular formula	C17H26O4

Structure

Classification

Send Inquiry Safety information

About 1H-Indene-4-carboxaldehyde,7-(acetyloxy)-2,3,5,6,7,7a-hexahydro-3-(hydroxymethyl)-1,1,3,5-tetramethyl-,[3S-(3a,5a,7a,7aa)]-

1H-Indene-4-carboxaldehyde,7-(acetyloxy)-2,3,5,6,7,7a-hexahydro-3-(hydroxymethyl)-1,1,3,5-tetramethyl-,[3S-(3a,5a,7a,7aa)]- is a chemical compound registered under CAS number 173485-79-5, with the molecular formula C17H26O4 and a molecular weight of about 294.39 g/mol. It is also known as Botryenalol. ChemOLED supplies 1H-Indene-4-carboxaldehyde,7-(acetyloxy)-2,3,5,6,7,7a-hexahydro-3-(hydroxymethyl)-1,1,3,5-tetramethyl-,[3S-(3a,5a,7a,7aa)]- for laboratory research and bulk production; product code 1335195. Send an inquiry for purity, packaging, price and lead time.

CAS Number: 173485-79-5
Molecular Formula: C17H26O4
Molecular Weight: 294.39 g/mol

Synonyms

Botryenalol

Related Keywords

indene

acetyloxy

hexahydro

tetramethyl

hydroxymethyl

carboxaldehyde

Indene

NISTC17351289

17351-28-9

Benzenemethanol, 3,4,5-tris[[4-(dodecyloxy)phenyl]methoxy]-

161401-95-2

1-(hexylsulfanyl)-2,3,6-trimethylhept-6-en-4-yn-3-ol

102244-19-9

3,6,9,12-Tetraoxatricosanoic acid

173536-73-7

2-Oxazolamine,4,5-dihydro-N-(1,2,3,4-tetrahydro-2-naphthalenyl)-

102280-54-6

Copper, dichloro[N,N'-2,6-pyridinediylbis[acetamide]]-

64638-48-8

4-({2-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]hydrazino}methyl)phthalazin-1(2H)-one

N'-acetyl-N',2-dimethylpropanehydrazide

3-Hexanone, 5-hydroxy-, (S)-

L-Lysine,L-leucyl-L-lysyl-L-leucyl-L-lysyl-L-leucyl-L-lysyl-L-leucyl-L-lysyl-L-leucyl-L-lysyl-L-leucyl-L-lysyl-L-leucyl-L-lysyl-L-leucyl-L-lysyl-L-leucyl-L-lysyl-L-leucyl-L-lysyl-L-leucyl-L-lysyl-L-leucyl-L-lysyl-L-leucyl-L-lysyl-L-leucyl-L-lysyl-L-leucyl