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88181-16-2

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88181-16-2 Usage

Description

(3E)-hex-3-ene-3,4-diyldibenzene-4,1-diyl bis[bis(2-chloroethyl)(amidochlorophosphate)] is a complex chemical compound with a long and intricate molecular structure. It contains a carbon chain with a double bond in the third position, connected to a benzene ring, and another benzene ring connected to the first one through a diyl (carbon-carbon) bridge. Additionally, the compound includes two bis(2-chloroethyl)(amidochlorophosphate) groups, characterized by the presence of both chlorine and phosphate atoms.

Uses

Used in Organic Synthesis:
(3E)-hex-3-ene-3,4-diyldibenzene-4,1-diyl bis[bis(2-chloroethyl)(amidochlorophosphate)] is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure and the potential reactivity of its functional groups make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Chemical Research:
(3E)-hex-3-ene-3,4-diyldibenzene-4,1-diyl bis[bis(2-chloroethyl)(amidochlorophosphate)] is used as a research compound in chemical laboratories to study its properties and reactivity. Its complex structure and functional groups provide opportunities for investigating new reaction pathways, mechanisms, and the development of novel synthetic methods.
Used in Pharmaceutical Development:
(3E)-hex-3-ene-3,4-diyldibenzene-4,1-diyl bis[bis(2-chloroethyl)(amidochlorophosphate)] is used as a starting material or intermediate in the development of new pharmaceuticals. Its unique structure and functional groups can be exploited to design and synthesize new drug candidates with potential therapeutic applications.
Used in Agrochemical Formulation:
(3E)-hex-3-ene-3,4-diyldibenzene-4,1-diyl bis[bis(2-chloroethyl)(amidochlorophosphate)] is used as a key component in the formulation of agrochemicals, such as pesticides and herbicides. Its reactivity and functional groups can be utilized to create new active ingredients with improved efficacy and selectivity for crop protection.
Used in Specialty Chemicals Production:
(3E)-hex-3-ene-3,4-diyldibenzene-4,1-diyl bis[bis(2-chloroethyl)(amidochlorophosphate)] is used as a raw material in the production of specialty chemicals, such as dyes, pigments, and polymers. Its unique structure and functional groups can contribute to the development of new materials with enhanced properties and performance.

Check Digit Verification of cas no

The CAS Registry Mumber 88181-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,8 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88181-16:
(7*8)+(6*8)+(5*1)+(4*8)+(3*1)+(2*1)+(1*6)=152
152 % 10 = 2
So 88181-16-2 is a valid CAS Registry Number.

88181-16-2SDS

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 N-[[4-[(E)-4-[4-[bis(2-chloroethyl)amino-chlorophosphoryl]oxyphenyl]hex-3-en-3-yl]phenoxy]-chlorophosphoryl]-2-chloro-N-(2-chloroethyl)ethanamine

1.2 Other means of identification

Product number -
Other names Diethylstilboestryl-bis-[di-(2-chlor-ethyl)-phosphoramid-chlorid]

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:88181-16-2 SDS

88181-16-2Relevant articles and documents

Phosphorus-Nitrogen Compounds. 24. Phosphoramide Mustard Carrier Derivatives

Cates, Lindley A.,Li, Ven-Shun,Powell, Douglas R.,Helm, Dick van der

, p. 397 - 401 (2007/10/02)

Diethylstilbestrol, psoralen, and propranolol were used as potential carrier molecules for selective concentrations of a nitrogen mustard moiety in breast, skin, and lung tissues, respectively.The propranolol derivative gave two racemic mixtures, which we

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