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2-Benzyloxybenzaldehyde

Product Name
2-Benzyloxybenzaldehyde
CAS No.
5896-17-3
Chemical Name
2-Benzyloxybenzaldehyde
Synonyms
CCY1a;AKOS AU36-M26;ASISCHEM N43068;2-Benzyloxybenzaldeh;OTAVA-BB BB7018801948;2-BENZYLOXYBENZALDEHYDE;2-BENZYLOXY BEZALDEHYDE;O-(BENZYLOXY)BENZALDEHYDE;2- Benxyloxy benzaldehyde;2-Benzyloxybenzaldehyde,98%
CBNumber
CB4363211
Molecular Formula
C14H12O2
Formula Weight
212.24
MOL File
5896-17-3.mol
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2-Benzyloxybenzaldehyde Property

Melting point:
46-47°C
Boiling point:
326 °C (lit.)
Density 
1.339 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.6(lit.)
Flash point:
>230 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Chloroform, Methanol (Slightly)
form 
Liquid
Specific Gravity
1.339
color 
Colorless to yellow
Water Solubility 
Insoluble in water.
Sensitive 
Air Sensitive
BRN 
780307
InChI
InChI=1S/C14H12O2/c15-10-13-8-4-5-9-14(13)16-11-12-6-2-1-3-7-12/h1-10H,11H2
InChIKey
PBEJTRAJWCNHRS-UHFFFAOYSA-N
SMILES
C(=O)C1=CC=CC=C1OCC1=CC=CC=C1
CAS DataBase Reference
5896-17-3(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
Safety Statements 
22-24/25
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29124990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H332Harmful if inhaled

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
499749
Product name
2-Benzyloxybenzaldehyde
Purity
98%
Packaging
10ml
Price
$55.4
Updated
2023/06/20
Sigma-Aldrich
Product number
499749
Product name
2-Benzyloxybenzaldehyde
Purity
98%
Packaging
50ml
Price
$176
Updated
2022/05/15
TCI Chemical
Product number
B1653
Product name
2-Benzyloxybenzaldehyde
Purity
>98.0%(GC)
Packaging
5g
Price
$25
Updated
2025/07/31
TCI Chemical
Product number
B1653
Product name
2-Benzyloxybenzaldehyde
Purity
>98.0%(GC)
Packaging
25g
Price
$69
Updated
2025/07/31
TRC
Product number
B411008
Product name
2-(Benzyloxy)benzaldehyde
Packaging
5g
Price
$70
Updated
2021/12/16
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2-Benzyloxybenzaldehyde Chemical Properties,Usage,Production

Chemical Properties

Clear pale yellow liquid

Uses

2-Benzyloxybenzaldehyde is used as an organic chemical synthesis intermediate.

Uses

2-Benzyloxybenzaldehyde may be used in the synthesis of:

  • 2-benzyloxy-2′-hydroxy-3′,4′,6′-trimethoxychalcone
  • N2-(2-benzyloxy)benzylidenyl isonicotinic acid hydrazide
  • 2-hydroxy-2′-methoxybenzophenone
  • 2′-hydroxy-5,6,7-trimethoxyflavone

General Description

2-Benzyloxybenzaldehyde is a benzaldehyde derivative. It undergoes enantioselective cyanoformylation with ethyl cyanoformate in the presence of a vanadium(V) chiral salen complex and imidazole to form the corresponding cyanohydrin carbonate.

Synthesis

100-44-7

90-02-8

5896-17-3

(Preparation of 2-benzyloxybenzaldehyde) 185 g of N,N-dimethylformamide (DMF) and 82.8 g (0.6 mol) of anhydrous potassium carbonate were added to a three-necked flask, and 61 g (0.5 mol) of salicylaldehyde was added slowly dropwise under stirring. Subsequently, the reaction system was warmed up to 50 °C, and 75.9 g (0.6 mol) of benzyl chloride was slowly added dropwise at this temperature for a controlled dropwise time of 1 hour. After the dropwise addition was completed, the reaction mixture was warmed up to 70 °C and the reaction was continued with stirring for 2 hours. Upon completion of the reaction, the mixture was transferred to a partition funnel and washed sequentially with 185 g of toluene and 330 g of water. The organic phases were combined and the solvent was removed by distillation under reduced pressure (internal temperature 90 °C, pressure 10 mmHg) to give 104.5 g of the brown liquid product 2-benzyloxybenzaldehyde, which was analyzed to have a purity of 97.9% and a yield of 96.5%.

References

[1] Organic and Biomolecular Chemistry, 2016, vol. 14, # 9, p. 2625 - 2636
[2] Patent: US6603029, 2003, B1
[3] Organic and Biomolecular Chemistry, 2017, vol. 15, # 17, p. 3648 - 3661
[4] Patent: CN108822095, 2018, A. Location in patent: Paragraph 0121; 0122; 0123
[5] Tetrahedron, 2015, vol. 71, # 33, p. 5217 - 5228

2-Benzyloxybenzaldehyde Preparation Products And Raw materials

Raw materials

Preparation Products

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2-Benzyloxybenzaldehyde Suppliers

TOKYO CHEMICAL INDUSTRY CO., LTD.
Tel
03-36680489
Fax
03-3668-0520
Email
Sales-JP@TCIchemicals.com
Country
Japan
ProdList
28387
Advantage
80
TCI Japan
Tel
--
Fax
--
Email
@TCIchemicals.com
Country
Japan
ProdList
2741
Advantage
58
K. Sakai & Co., Ltd.
Tel
--
Fax
--
Email
em@ksakai.co.jp
Country
Japan
ProdList
957
Advantage
58
Wako Pure Chemical Industries, Ltd.
Tel
--
Fax
--
Email
labchem-tec@wako-chem.co.jp
Country
Japan
ProdList
6819
Advantage
80
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View Lastest Price from 2-Benzyloxybenzaldehyde manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
2-Benzyloxybenzaldehyde 5896-17-3
Price
US $0.00-0.00/g
Min. Order
10mg
Purity
99%HPLC
Supply Ability
2000tons
Release date
2020-01-15
Career Henan Chemical Co
Product
2-Benzyloxybenzaldehyde 5896-17-3
Price
US $1.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
200kg
Release date
2019-08-29

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