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(1aS,2R,3S,11dR)-1a,2,3,11d-tetrahydrobenzo[5,6]phenanthro[3,4-b]oxirene-2,3-diol is a complex organic molecule with a unique structure, featuring a benzene ring fused to a phenanthrene ring, an oxirene group, and two hydroxyl (OH) groups attached to the carbon atoms. As a chiral molecule with four stereocenters, its IUPAC name indicates the specific arrangement of atoms and stereochemistry. (1aS,2R,3S,11dR)-1a,2,3,11d-tetrahydrobenzo[5,6]phenanthro[3,4-b]oxirene-2,3-diol may have potential applications in various fields such as organic synthesis, medicinal chemistry, or materials science, but further research is necessary to explore its properties and uses.

75410-89-8

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75410-89-8 Usage

Uses

Used in Organic Synthesis:
(1aS,2R,3S,11dR)-1a,2,3,11d-tetrahydrobenzo[5,6]phenanthro[3,4-b]oxirene-2,3-diol is used as a key intermediate in organic synthesis for the development of novel compounds with potential applications in various industries.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (1aS,2R,3S,11dR)-1a,2,3,11d-tetrahydrobenzo[5,6]phenanthro[3,4-b]oxirene-2,3-diol is utilized as a building block for the design and synthesis of new pharmaceutical agents, potentially targeting various diseases and medical conditions.
Used in Materials Science:
(1aS,2R,3S,11dR)-1a,2,3,11d-tetrahydrobenzo[5,6]phenanthro[3,4-b]oxirene-2,3-diol is employed in materials science for the creation of advanced materials with unique properties, such as improved strength, stability, or specific interactions with other molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 75410-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,1 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75410-89:
(7*7)+(6*5)+(5*4)+(4*1)+(3*0)+(2*8)+(1*9)=128
128 % 10 = 8
So 75410-89-8 is a valid CAS Registry Number.

75410-89-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (1aS,2R,3S,11dR)-1a,2,3,11d-Tetrahydrobenzo[5,6]phenanthro[3,4-b] oxirene-2,3-diol

1.2 Other means of identification

Product number -
Other names rac-3-propylisochroman-1-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:75410-89-8 SDS

75410-89-8Relevant academic research and scientific papers

An Efficient Synthesis of the Highly Tumorigenic anti-Diol Epoxide Derivative of Benzophenanthrene

Pataki, John,Raddo, Pasquale Di,Harvey, Ronald G.

, p. 840 - 844 (2007/10/02)

Synthesis of the potent tumorigen trans-3,4-dihydroxy-anti-1,2,3,4-tetrahydrobenzophenanthrene (1) in relatively few steps and superior overall yield is described.The method entails synthesis of the key intermediate 3-hydroxybenzophenanthrene (7b) v

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