5-tert-Butyl-1,3-bis(chloromethyl)-2-methylbenzene

Base Information

Chemical Name:5-tert-Butyl-1,3-bis(chloromethyl)-2-methylbenzene
CAS No.:35322-87-3
Molecular Formula:C13H18Cl2
Molecular Weight:
Hs Code.:
DSSTox Substance ID:DTXSID50505979
Wikidata:Q82361486
Mol file:35322-87-3.mol

Synonyms:5-tert-Butyl-1,3-bis(chloromethyl)-2-methylbenzene;35322-87-3;DTXSID50505979

Suppliers and Price of 5-tert-Butyl-1,3-bis(chloromethyl)-2-methylbenzene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of 5-tert-Butyl-1,3-bis(chloromethyl)-2-methylbenzene

Chemical Property:

XLogP3:4.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:3
Exact Mass:244.0785560
Heavy Atom Count:15
Complexity:181

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C=C(C=C1CCl)C(C)(C)C)CCl

Technology Process of 5-tert-Butyl-1,3-bis(chloromethyl)-2-methylbenzene

There total 2 articles about 5-tert-Butyl-1,3-bis(chloromethyl)-2-methylbenzene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 98-51-1
4-tert-butyltoluene

: 35322-87-3
2,6-bis(chloromethyl)-4-tert-butyl-toluene

Guidance literature:: (chloromethylation);
DOI:10.1039/P19720000151

Reference yield:

: 35322-87-3
2,6-bis(chloromethyl)-4-tert-butyl-toluene

Guidance literature:

Reference yield:

: 35322-87-3
2,6-bis(chloromethyl)-4-tert-butyl-toluene

: 191862-56-3
2-methyl-5-tert-butyl-1,3-benzenedicarboxaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 2 h / Heating

2: N,N-dimethyl-4-nitrosoaniline, aq. NaOH / ethanol / 1.5 h / Ambient temperature

With sodium hydroxide; p-dimethylaminonitrosobenzene; In ethanol;
DOI:10.1016/S0040-4020(99)00055-1