1. Home
  2. Benzene, 1,1'-(chloroethenylidene)bis[4-chloro-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzene, 1,1'-(chloroethenylidene)bis[4-chloro-

ClC=C(c1ccc(cc1)Cl)c1ccc(cc1)Cl Request for Quotation
Chemical Name: Benzene, 1,1'-(chloroethenylidene)bis[4-chloro-
CAS Number: 1022-22-6
Product Number: AG007G68(AGN-PC-0JM31O)
Synonyms:
MDL No:
Molecular Formula: C14H9Cl3
Molecular Weight: 283.5803

Identification/Properties

Computed Properties
Molecular Weight:
283.576g/mol
XLogP3:
6.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
281.977g/mol
Monoisotopic Mass:
281.977g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
235
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


P,p′-DDMU, also known as p,p′-Dimethoxypropane, is a versatile chemical compound widely used in various chemical synthesis processes. This clear, colorless liquid serves as a valuable reagent in organic chemistry due to its unique properties and applications.In chemical synthesis, p,p′-DDMU is primarily employed as a protecting group reagent for alcohols. By reacting with the hydroxyl groups of alcohols, p,p′-DDMU forms stable acetals, thereby temporarily shielding the alcohol functionality from unwanted reactions during complex synthesis processes. This protective role allows chemists to selectively modify other functional groups present in the molecule without affecting the alcohol group, ultimately enabling the precise control of chemical reactions.Furthermore, p,p′-DDMU is commonly used in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its compatibility with a wide range of functional groups, mild reaction conditions, and ease of removal make it a preferred choice in organic synthesis laboratories worldwide. The versatile nature of p,p′-DDMU contributes to its widespread applicability in the development of new molecules and compounds across different industries.