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4-Tert-butyldiphenylsiloxy-2-chloromethyl-6-hydroxy benzaldehyde

Base Information
  • Chemical Name:4-Tert-butyldiphenylsiloxy-2-chloromethyl-6-hydroxy benzaldehyde
  • CAS No.:378749-92-9
  • Molecular Formula:C24H25ClO3Si
  • Molecular Weight:424.999
  • Hs Code.:
  • DSSTox Substance ID:DTXSID401134741
4-Tert-butyldiphenylsiloxy-2-chloromethyl-6-hydroxy benzaldehyde

Synonyms:VNXFLNZDSPGBFQ-UHFFFAOYSA-N;DTXSID401134741;4-tert-butyldiphenylsiloxy-2-chloromethyl-6-hydroxy benzaldehyde;378749-92-9;2-(Chloromethyl)-4-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-6-hydroxybenzaldehyde

Suppliers and Price of 4-Tert-butyldiphenylsiloxy-2-chloromethyl-6-hydroxy benzaldehyde
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 4-Tert-butyldiphenylsiloxy-2-chloromethyl-6-hydroxy benzaldehyde
Chemical Property:
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:7
  • Exact Mass:424.1261489
  • Heavy Atom Count:29
  • Complexity:505
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)[Si](C1=CC=CC=C1)(C2=CC=CC=C2)OC3=CC(=C(C(=C3)O)C=O)CCl
Technology Process of 4-Tert-butyldiphenylsiloxy-2-chloromethyl-6-hydroxy benzaldehyde

There total 2 articles about 4-Tert-butyldiphenylsiloxy-2-chloromethyl-6-hydroxy benzaldehyde 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:
Guidance literature:
Multi-step reaction with 3 steps
1.1: POCl3 / 0.33 h / 25 °C
1.2: 93 percent / 2 h / 25 - 75 °C
2.1: 96 percent / BBr3 / CH2Cl2 / 20 h / 25 °C
3.1: 97 percent / imidazole / CH2Cl2; tetrahydrofuran / 12 h / 25 °C
With 1H-imidazole; boron tribromide; trichlorophosphate; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja011364+
Guidance literature:
Multi-step reaction with 2 steps
1: 96 percent / BBr3 / CH2Cl2 / 20 h / 25 °C
2: 97 percent / imidazole / CH2Cl2; tetrahydrofuran / 12 h / 25 °C
With 1H-imidazole; boron tribromide; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja011364+
Guidance literature:
With aminosulfonic acid; In tetrahydrofuran; water; dimethyl sulfoxide; at 0 ℃; for 0.5h;
DOI:10.1021/ja011364+
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