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Merck
CN

163953

3-苄氧基-4-甲氧基苯甲醛

98%

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关于此项目

线性分子式:
C6H5CH2OC6H3(OCH3)CHO
化学文摘社编号:
分子量:
242.27
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
228-752-7
MDL number:
Assay:
98%
Form:
solid
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Quality Level

assay

98%

form

solid

mp

61-64 °C (lit.)

functional group

aldehyde, phenyl

SMILES string

COc1ccc(C=O)cc1OCc2ccccc2

InChI

1S/C15H14O3/c1-17-14-8-7-13(10-16)9-15(14)18-11-12-5-3-2-4-6-12/h2-10H,11H2,1H3

InChI key

VQVQZFHUXRSRBZ-UHFFFAOYSA-N

Application

3-Benzyloxy-4-methoxybenzaldehyde was used in the synthesis of (+)-9-benzyloxy-α-dihydrotetrabenazine. It was also used in total synthesis of (-)-galipeine.


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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历史批次信息供参考:

分析证书(COA)

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Chunyi Liu et al.
Chirality, 25(4), 215-223 (2013-03-28)
This article reports, for the first time, on the absolute configuration of (+)-9-benzyloxy-α-dihydrotetrabenazine (8), as determined from the perspective of X-ray crystallography. Compound 8 was prepared by a six-step reaction using 3-benzyloxy-4-methoxybenzaldehyde (1) as a starting material. The X-ray crystal
The enantioselective total synthesis of alkaloid (-)-galipeine.
Yang P-Y and Zhou Y-G.
Tetrahedron Asymmetry, 15(7), 1145-1149 (2004)



全球贸易项目编号

货号GTIN
WH0001673M1-100UG04061832742199
HPA004335-25UL04061842721894
P5687-.2ML04061837861550
WH0000055M1-100UG04061829595449
WH0005660M1-100UG04061831647525
SAB4502422-100UG04061835716401
SAB2101911-100UL04061836144654
HPA004335-100UL04061836308988
HPA004426-100UL04061836309015
HPA004426-25UL04061842721931
163953-10G04061838747846
163953-50G04061831828634