4-Benzyloxybenzalde...

4-Benzyloxybenzaldehyde 4397-53-9 Large in promotion

4-Benzyloxybenzaldehyde 4397-53-9 Large in promotion

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1 Kilogram

Negotiable

  • Min.Order :1 Kilogram
  • Purity: 98.00%
  • Payment Terms : T/T,Other

Keywords

4-Benzyloxybenzaldehyde 4397-53-9 P-BENZYLOXY BENZALDEYHDE

Quick Details

  • Appearance:creamish to yellow crystalline powder
  • Application:4-Benzyloxybenzaldehyde is a position isomer of the adenylyl cyclase activator 2-Benzyloxybenzaldehyde. 4-Benzyloxybenzaldehyde also has much less potent anticancer activity against HL-60 cells that i
  • PackAge:drums
  • ProductionCapacity:20|Metric Ton|Month
  • Storage:dry and cool
  • Transportation:air, courier and sea

Superiority:

4-Benzyloxybenzaldehyde Basic information

Product Name: 4-Benzyloxybenzaldehyde
Synonyms: AKOS AU36-M28;AKOS BBS-00003143;4-BENZYLOXYBENZALDEHYDE;LABOTEST-BB LT00233210;ASISCHEM R39515;TIMTEC-BB SBB000526;P-(BENZYLOXY)BENZALDEHYDE;P-BENZYLOXY BENZALDEYHDE
CAS: 4397-53-9
MF: C14H12O2
MW: 212.24
EINECS: 224-527-2
Product Categories: FINE Chemical & INTERMEDIATES;Aromatic Aldehydes & Derivatives (substituted);Benzaldehyde (Building Blocks for Liquid Crystals);Building Blocks for Liquid Crystals;Functional Materials;Aldehydes;C10 to C21;Carbonyl Compounds;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File: 4397-53-9.mol

 

Details:


4-Benzyloxybenzaldehyde Chemical Properties

mp  71-74 °C(lit.)

bp  197-199 °C (11 mmHg) 
Fp  197-199°C/20mm
Water Solubility  insoluble
Sensitive  Air Sensitive
BRN  1242385
CAS DataBase Reference 4397-53-9(CAS DataBase Reference)
NIST Chemistry Reference Benzyl 4-formylphenyl ether(4397-53-9)
EPA Substance Registry System Benzaldehyde, 4-(phenylmethoxy)-(4397-53-9)



Safety Information

Safety Statements  24/25
WGK Germany  3

F  9-23
HazardClass  IRRITANT
HS Code  29124900

Chemical Properties creamish to yellow crystalline powder
Usage 4-Benzyloxybenzaldehyde is a position isomer of the adenylyl cyclase activator 2-Benzyloxybenzaldehyde. 4-Benzyloxybenzaldehyde also has much less potent anticancer activity against HL-60 cells that i ts isomeric counterpart.


 

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