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Merck
CN

226076

苯甲醛二甲缩醛

99%

别名:

α,α-二甲氧基甲苯

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线性分子式:
C6H5CH(OCH3)2
化学文摘社编号:
分子量:
152.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-413-0
Beilstein/REAXYS Number:
2044501
MDL number:
Assay:
99%
Form:
liquid
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产品名称

苯甲醛二甲缩醛, 99%

InChI key

HEVMDQBCAHEHDY-UHFFFAOYSA-N

InChI

1S/C9H12O2/c1-10-9(11-2)8-6-4-3-5-7-8/h3-7,9H,1-2H3

SMILES string

COC(OC)c1ccccc1

assay

99%

form

liquid

refractive index

n20/D 1.493 (lit.)

bp

87-89 °C/18 mmHg (lit.)

density

1.014 g/mL at 25 °C (lit.)

functional group

acetal
ether
phenyl

Quality Level

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Application

苯甲醛二甲基缩醛用作构建硒代羰基化合物的有效试剂

General description

研究了活性溴在80°下从苯甲醛二甲缩醛中萃取α-氢原子的反应

苯甲醛二甲缩醛是由苯甲醛和甲醇缩合反应获得。它被用作保护基团。

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

156.2 °F - closed cup

flash_point_c

69 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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1151. Polar influences in radical reactions. Part IV. The abstraction of benzylic hydrogen atoms from substituted benzyl methyl ethers and benzaldehyde dimethyl acetals by atomic bromine.
Huang RL and Lee KH.
Journal of the Chemical Society, 5963-5969 (1964)
One-pot synthesis of orthogonally protected sugars through sequential base-promoted/acid-catalyzed steps: A solvent-free approach with self-generation of a catalytic species
Traboni S, et al.
Tetrahedron Letters, 60, 1777-1780 (2019)
Tetrahedron Letters, 33, 7865-7865 (1992)
N Sakairi et al.
Carbohydrate research, 246, 61-73 (1993-08-17)
Treatment of phenyl alpha-maltoside with an excess of alpha, alpha-dimethoxytoluene in the presence of (+)-10-camphorsulfonic acid, followed by partial hydrolysis to remove unstable acyclic acetal substituents, gave phenyl 3,2':4',6'-di-O-benzylidene-alpha-maltoside. Thus, one of the benzylidene groups formed an eight-membered cyclic acetal
Simona Matrella et al.
Macromolecular bioscience, 15(7), 927-940 (2015-03-18)
Intrinsic antimicrobial thermoplastic A(BC)n copolymers (n = 1, 2, 4), where A was poly(ethylene glycol) (PEG), BC was a random chain of methylmethacrylate (MMA), and alkyl-aminoethyl methacrylate (AAEMA), were synthesized and the antimicrobial activity and hemolyticity were evaluated on plaques obtained by

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