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1,4-Ethano-1H-indene, octahydro- is a chemical compound with the molecular formula C11H18. It is a cyclic hydrocarbon, specifically a derivative of indene, which is a tricyclic aromatic hydrocarbon. 1,4-Ethano-1H-indene, octahydro- is characterized by its unique structure, where an ethano bridge connects two carbon atoms in the indene molecule, and the molecule is fully saturated with eight hydrogen atoms. It is an organic compound with potential applications in the synthesis of various chemical products and materials. Due to its complex structure, it is important to handle 1,4-Ethano-1H-indene, octahydro- with care, following proper safety protocols.

60887-91-4

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60887-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60887-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,8 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 60887-91:
(7*6)+(6*0)+(5*8)+(4*8)+(3*7)+(2*9)+(1*1)=154
154 % 10 = 4
So 60887-91-4 is a valid CAS Registry Number.

60887-91-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-Ethano-1H-indene, octahydro-

1.2 Other means of identification

Product number -
Other names 2,4-bishomobrexane

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:60887-91-4 SDS

60887-91-4Downstream Products

60887-91-4Relevant academic research and scientific papers

Novel Rearrangement of 5,6-Disubstituted Bicyclooctan-2-ones with AlCl3. Application to Total Synthesis of (+/-)-5-Oxosilphiperfol-6-ene and (+/-)-Silphiperfol-6-ene

Kakiuchi, Kiyomi,Ue, Masaki,Tsukahara, Hiroshi,Shimizu, Toshihiro,Miyao, Tomoya,et al.

, p. 3707 - 3712 (2007/10/02)

The acid-catalyzed rearrangement of bi- and tricyclic cyclobutyl ketones 8-20 having a bicyclooctan-2-one moiety with AlCl3 was studied to elucidate the scope and limitations of the novel rearrangement by which the tricyclic ketone 1 gave the angul

Reductive Rearrangement with Hydride Transfer of Linearly and Angularly Fused Triquinanes

Kakiuchi, Kiyomi,Ue, Masaki,Kumanoya, Shuichi,Takeuchi, Hideyuki,Tobe, Yoshito,Odaira, Yoshinobu

, p. 1479 - 1482 (2007/10/02)

Relationship between linearly and angularly fused triquinanes is elucidated by reductive rearrangements with hydride transfer of tricyclo2,6>undecan-1-ol, tricyclo1,5>undecan-6-ols, and tricyclo1,5>undecan-11-ol.

Acid-Catalyzed Rearrangements of - and Propellanes, Tricyclo1,5>undecanes, and Tricyclo1,5>undecanes

Kakiuchi, Kiyomi,Ue, Masaki,Wakaki, Itsuyo,Tobe, Yoshito,Odaira, Yoshinobu,et al.

, p. 281 - 287 (2007/10/02)

Acid-catalyzed rearrangements of propellanols 2x and 2n, propellanol (3b), tricyclo1,5>-undecanes 4b-d and 5, and tricyclo1,5>undecanes 6a,b were studied.Tricycloundecanes 4d and 6b rearranged under CF3S

ACID CATALYZED RING CONTRACTIONS IN ENDO-2,8-TRIMETHYLENE-CIS-BICYCLOOCTYL CATIONS TO METHYLPERHYDROTRIQUINACENES. ONE OF THE METHYL EXTRUSION PROCESSES IN THE TRICYCLOUNDECANE REARRANGEMENT

Fujikura, Yoshiaki,Takaishi, Naotake,Inamoto, Yoshiaki

, p. 4465 - 4478 (2007/10/02)

Sulfuric acid catalyzed ring contractions with extrusion of a methyl group were examined for alcohol and olefin derivatives (28-31) of endo-2,8-trimethylene-cis-bicyclooctane (11), which was one of the two possible progenitors, among altogether 69

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