3,5-Di-tert-Butylsalicylaldehyde CAS 37942-07-7 Purity >99.0% (GC) Factory High Quality

Chemical Name: 3,5-Di-tert-Butylsalicylaldehyde 

CAS: 37942-07-7

Purity: >99.0% (GC)

Appearance: Light Yellow to Yellow Powder or Crystals

High Quality, Commercial Production

E-Mail: alvin@ruifuchem.com

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Chemical Properties:

Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement. Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture.Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of 3,5-Di-tert-Butylsalicylaldehyde (CAS: 37942-07-7) with high quality, commercial production. Welcomed to order.
Item Specifications
Appearance Light Yellow to Yellow Powder or Crystals
Purity / Analysis Method >99.0% (GC)
Melting Point 58.0~63.0℃
Loss on Drying <1.00%
Total Impurities <1.00%
1 H NMR Spectrum Consistent With Structure
Test Standard Enterprise Standard
Usage Pharmaceutical Intermediates

Description:

Specifications:

Package & Storage:

Chemical Name 3,5-Di-tert-Butylsalicylaldehyde
Synonyms 3,5-Di-tert-butyl-2-Hydroxybenzaldehyde
CAS Number 37942-07-7
CAT Number RF-PI1615
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C15H22O2
Molecular Weight 234.34  
Density   1.006±0.06 g/cm3
Solubility Soluble in Methanol
Brand Ruifu Chemical

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Application:

3,5-Di-tert-Butylsalicylaldehyde (CAS: 37942-07-7) can be used as an organic synthesis intermediate and pharmaceutical intermediate. 3,5-Di-tert-Butylsalicylaldehyde is used in the synthesis of Mn(III)-salen complex and its diamino precursor 5,6-diamino-5,6-dideoxy-1,2-O-isopropylidene-3-O-methyl-β-L-idofuranose, chiral Schiff base ligand for an enantioselective copper-catalyzed addition of phenyl acetylene to imines, chiral oxazolidine ligand for the enantioselective addition of diethyl zinc to aldehydes and tin Schiff base complexes with histidine analogues. It has antibacterial activity and is used in the preparation nickel complexes. It is structurally related to 3,5-di-t-Butylcatechol (DTCAT) but is not as potent an activator of rat skeletal muscle ryanodine receptor Ca2+ channel (RyRC).

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