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6952-36-9

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  • 1-(anilinomethylidene)-7-[8-(anilinomethylidene)-1,6-dihydroxy-3-methyl-7-oxo-5-propan-2-yl-naphthalen-2-yl]-3,8-dihydroxy-6-methyl-4-propan-2-yl-naphthalen-2-one

    Cas No: 6952-36-9

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  • 1-(anilinomethylidene)-7-[8-(anilinomethylidene)-1,6-dihydroxy-3-methyl-7-oxo-5-propan-2-yl-naphthalen-2-yl]-3,8-dihydroxy-6-methyl-4-propan-2-yl-naphthalen-2-one cas 6952-36-9

    Cas No: 6952-36-9

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6952-36-9 Usage

Anilinomethylidene groups

These groups are derived from aniline, an aromatic amine, and are characterized by the presence of a nitrogen atom bonded to a phenyl ring. They are part of the complex molecular structure of the compound.

Hydroxyl groups

These are functional groups containing an oxygen and hydrogen atom (-OH). They are present at the 1, 3, and 8 positions of the naphthalene rings, contributing to the compound's polarity and potential for hydrogen bonding.

Methyl groups

These are small alkyl groups consisting of a single carbon atom bonded to three hydrogen atoms (-CH3). They are present at the 6 and 3 positions of the naphthalene rings, providing steric hindrance and affecting the compound's reactivity.

Naphthalene rings

The compound contains two naphthalene rings, which are fused aromatic hydrocarbons consisting of two six-membered carbon rings. These rings contribute to the compound's stability and aromaticity.

Ketone group

The compound features a carbonyl group (C=O) at the 7 position of one of the naphthalene rings. This group is important for the compound's reactivity, as it can participate in various chemical reactions, such as nucleophilic addition and enolization.

Propan-2-yl group

This is an alkyl group derived from propane, consisting of three carbon atoms and seven hydrogen atoms. It is attached to the 5 position of one of the naphthalene rings, providing additional steric hindrance and affecting the compound's reactivity.

Oxo group

The compound contains an oxo group (C=O) at the 7 position of the second naphthalene ring, further contributing to its reactivity and potential for chemical reactions.

Molecular complexity

The compound's long and specific molecular structure, with multiple functional groups and substituents, makes it a complex organic molecule. This complexity affects its chemical properties, reactivity, and potential applications.

Potential applications

Due to its unique structure and functional groups, the compound may have various potential applications in fields such as pharmaceuticals, materials science, or chemical research. However, further investigation and experimentation would be required to determine its specific uses and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 6952-36-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6952-36:
(6*6)+(5*9)+(4*5)+(3*2)+(2*3)+(1*6)=119
119 % 10 = 9
So 6952-36-9 is a valid CAS Registry Number.

6952-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1Z)-1-(anilinomethylidene)-7-[(8Z)-8-(anilinomethylidene)-1,6-dihydroxy-3-methyl-7-oxo-5-propan-2-ylnaphthalen-2-yl]-3,8-dihydroxy-6-methyl-4-propan-2-ylnaphthalen-2-one

1.2 Other means of identification

Product number -
Other names Gossypoldianil

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:6952-36-9 SDS

6952-36-9Downstream Products

6952-36-9Relevant articles and documents

Synthesis, Structures, and Acute Toxicity of Gossypol Nonsymmetrical Aldehyde Derivatives

Tilyabaev,Kamaev,Vypova,Yuldashev,Ibragimov,Talipov

experimental part, p. 390 - 395 (2011/05/06)

Nonsymmetrical aldehyde derivatives of gossypol, a yellow polyphenolic pigment of cottonseed, were synthesized by reactions with ammonia, aniline, 4-aminoantipyrine, and barbituric acid. Their structures were determined by UV spectrophotometry and IR and

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