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9,10,10a,11a-tetrahydrotriphenyleno[1,2-b]oxirene-9,10-diol is a complex organic compound with a unique molecular structure. It is characterized by a tetrahydrotriphenylene core, which is a type of polycyclic aromatic hydrocarbon, and an oxirene (oxirane) ring fused to it. The compound also features two hydroxyl groups attached to the 9 and 10 positions, which contribute to its polarity and potential reactivity. This chemical is of interest in the field of organic chemistry, particularly for its potential applications in the synthesis of more complex molecules and materials. Its specific properties, such as solubility, stability, and reactivity, would be of interest to researchers studying its behavior and potential uses in various chemical processes.

68151-06-4

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68151-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68151-06-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,5 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 68151-06:
(7*6)+(6*8)+(5*1)+(4*5)+(3*1)+(2*0)+(1*6)=124
124 % 10 = 4
So 68151-06-4 is a valid CAS Registry Number.

68151-06-4SDS

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 AC1L49LD

1.2 Other means of identification

Product number -
Other names -

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

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More Details:68151-06-4 SDS

68151-06-4Downstream Products

68151-06-4Relevant academic research and scientific papers

Stereocontrolled synthesis of syn- and anti-diol epoxide metabolites of triphenylene

Koreeda, Masato,Gopalaswamy, Ramesh,Yang, Jinhai,Tuinman, Roeland J.

, p. 8267 - 8270 (2007/10/03)

The synthesis of both syn- and anti-diol epoxide metabolites of triphenylene has been achieved under complete stereochemical control commencing with commercially available 9-phenanthrol in 18% (9 steps) and 37% (8 steps) overall yields, respectively. The exceptionally high stereoselectivity of the dimethyldioxirane oxidation of trans-dihydrodiol having the quasi-diaxially disposed hydroxyl groups is particularly noteworthy.

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