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3,3'-Diallyldiethylstilbestrol (DDES) is a synthetic non-steroidal estrogen that is structurally similar to the naturally occurring hormone estradiol. It is a derivative of diethylstilbestrol (DES), with the addition of allyl groups at the 3,3' positions. DDES has been used in various applications, including as a growth promoter in livestock and as a potential contraceptive. However, due to its potential health risks and endocrine-disrupting properties, its use has been restricted or banned in many countries. The compound can have estrogenic effects on the body, potentially leading to reproductive and developmental issues, and it has been linked to an increased risk of certain cancers. As a result, research and regulatory focus has shifted towards understanding and mitigating the impacts of DDES and similar compounds on human health and the environment.

4870-88-6

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4870-88-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4870-88-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4870-88:
(6*4)+(5*8)+(4*7)+(3*0)+(2*8)+(1*8)=116
116 % 10 = 6
So 4870-88-6 is a valid CAS Registry Number.

4870-88-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(E)-4-(4-hydroxy-3-prop-2-enylphenyl)hex-3-en-3-yl]-2-prop-2-enylphenol

1.2 Other means of identification

Product number -
Other names 3,3'-diallyl-diethylstilbestrol

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:4870-88-6 SDS

4870-88-6Relevant academic research and scientific papers

Bisphenol-based epoxy compound using thiol-ene reaction and method for preparing the same, and composite of organic-inorganic materials comprising a cured product thereof and method for preparing the composite

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Paragraph 0136-0138, (2017/08/24)

The present invention relates to a bisphenol-based epoxy compound having an alkoxysilylalkyl-S-alkyl group and a method for preparing the same, a composite of organic-inorganic materials comprising the cured product and a method for preparing the composite. The novel bisphenol-based epoxy compound can provide a composite which shows improved thermal resistance and thermal expansion properties and has excellent hardness when being used for manufacturing high-integration and high-performance electronic components such as a next-generation semiconductor substrate and PCB.COPYRIGHT KIPO 2017

Bisphenol-based epoxy compound having alkoxysilyl group and method for preparing the same, and composite of organic-inorganic materials comprising a cured product thereof and method for preparing the composite

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Paragraph 0128-0130, (2017/06/13)

The present invention relates to a bisphenol-based epoxy compound having an alkoxysilyl group and a method for preparing the same, and a composite of organic-inorganic materials comprising the cured products thereof and a method for preparing the composite. The novel bisphenol-based epoxy compound shows improved thermal resistance and thermal expansion properties, and excellent hardness when used for manufacturing high integration and performance electronic components such as a next generation semiconductor substrate and PCB.

Synthesis, cytotoxicity, and antiviral activities of new neolignans related to honokiol and magnolol

Amblard, Franck,Govindarajan, Baskaran,Lefkove, Benjamin,Rapp, Kimberly L.,Detorio, Mervi,Arbiser, Jack L.,Schinazi, Raymond F.

, p. 4428 - 4431 (2008/02/11)

A series of new bisphenol derivatives bearing allylic moieties were synthesized as potential analogs of honokiol and/or magnolol. Certain compounds exhibited specific anti-proliferation activity against SVR cells and moderate anti-HIV-1 activity in primary human lymphocytes. Compound 5h was the most potent compound and its anti-tumor activity was evaluated in vivo.

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