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The chemical compound "2,3,5,6,7,8,9,10-Octahydro-5-hydroxy-2,2,7,7,9-pentamethyl-5,9-methanobenzocycloocten-4(1H)-one" is a complex organic molecule with a unique structure. It is characterized by an octahydro (eight hydrogen atoms in a cyclic structure) and a pentamethyl (five methyl groups) pattern, which contribute to its stability and reactivity. The compound features a hydroxyl group at the 5-position, indicating the presence of an alcohol functional group, and a methano bridge connecting the benzene ring to the cyclooctene ring. This structure classifies it as a derivative of benzocyclooctenone, a type of aromatic compound with a cyclooctene ring fused to a benzene ring. The compound's specific arrangement of hydrogen and methyl groups, along with its hydroxyl and methano bridge, give it distinct chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

6244-16-2

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6244-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6244-16-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,4 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6244-16:
(6*6)+(5*2)+(4*4)+(3*4)+(2*1)+(1*6)=82
82 % 10 = 2
So 6244-16-2 is a valid CAS Registry Number.

6244-16-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name diisophor-2(7)-en-1-ol-3-one

1.2 Other means of identification

Product number -
Other names (1S,9R)-1-Hydroxy-5,5,9,11,11-pentamethyl-tricyclo[7.3.1.02,7]tridec-2(7)-en-3-one

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:6244-16-2 SDS

6244-16-2Relevant academic research and scientific papers

Diisophorone and Related Compounds, Part 27. Nucleophilic Reactions of 1-Halogenodiisophoranes

Kurzer, Frederick,Duffner, C. Richard

, p. 1314 - 1323 (2007/10/02)

The action of nucleophiles on 1-halogenodiisophoranes obtained by several methods from the corresponding 1-hydroxy or 1-alkoxy compounds, replaces their bridgehead 1-halogen by hydroxy, alkoxy or acetoxy groups.The semiquantitative results show that the h

7,10a-Methanocyclooctaindazoles: Diisophoranes Incorporating the Pyrazole Ring System

Kurzer, Frederick,Langer, Stanley S.

, p. 871 - 879 (2007/10/02)

Compounds of the novel 7,10a-methanocyclooctaindazole ring-system 5, 7 are obtained by the action of hydrazines on 1-chloro(or hydroxy)diisophor-2,7-en-3-ones 1-3.Their formulation agrees with their origin and their chemical and spectral characteristics.Analogous syntheses of two comparable ring-systems include the production of a substituted 7,10a-methanocyclooctabenzisoxazole 10 by a facile cyclodehydration of the oxime of diisophorone 9a, and that of the indole-analogue 13 by the action of aniline on diisophorone-1-carboxylic acid 11.

Di-isophorone and Related Compounds. Part 8. 1-Aminodi-isophorane Derivatives

Allen, Anthony A.,Kurzer, Frederick

, p. 617 - 626 (2007/10/02)

The interaction of 1-chlorodi-isophor-2(7)-en-3-one or its 5,11-bisnor-homologue with potassium phthalimide yields the corresponding 1-phthalimido-compounds, which are converted into the 1-amines on treatment with hydrazine, followed by hydrolysis. 1-Aminodi-isophor-2(7)-ene is not accessible by this route, but its N-acyl-derivatives are obtainable directly from 1-hydroxydi-isophor-2(7)-ene by the Ritter reaction; the 3-keto-analogue reacts similarly.Some properties of the novel 1-aminodi-isophoranes are described. - Keywords: Di-isophorones, 1-amino; Tricyclo2,7>tridecanes

Di-isophorone and Related Compounds. Part 5. 2,7-Epoxydi-isophoranes: Oxiran Cleavage by Perchloric Acid

Allen, Anthony A.,Kurzer, Frederick,Morgan, Alan R.

, p. 733 - 737 (2007/10/02)

Perchloric acid slowly converts 2,7-epoxy-1-hydroxydi-isophoran-3-one into 1,4-dihydroxydi-isophor-2(7)-en-3-one, the structure of which is in accord with its alternative formation from 2,7-epoxy-1-hydroxydi-isophorane-3,4-dione by reduction with zinc in

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