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D105937

1,2-二氢萘

Name: 1,2-二氢萘
Brand: ALDRICH

95%

别名:

1,2-二亚林, 3,4-二氢萘

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关于此项目

经验公式（希尔记法）:

C₁₀H₁₀

化学文摘社编号:

447-53-0

分子量:

130.19

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24893339

EC Number:

207-183-8

Beilstein/REAXYS Number:

1851372

MDL number:

MFCD00001672

Assay:

≥94.5% (GC), 95%

Form:

liquid

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属性

Quality Level

100

assay

≥94.5% (GC), 95%

form

liquid

refractive index

n20/D 1.582 (lit.)

bp

89 °C/16 mmHg (lit.)

mp

−8 °C (lit.)

density

0.997 g/mL at 25 °C (lit.)

SMILES string

C1Cc2ccccc2C=C1

InChI

1S/C10H10/c1-2-6-10-8-4-3-7-9(10)5-1/h1-3,5-7H,4,8H2

InChI key

KEIFWROAQVVDBN-UHFFFAOYSA-N

说明

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存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

152.6 °F - closed cup

flash_point_c

67 °C - closed cup

ppe

Eyeshields, 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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Desaturation and oxygenation of 1,2-dihydronaphthalene by toluene and naphthalene dioxygenase.

D S Torok et al.

Journal of bacteriology, 177(20), 5799-5805 (1995-10-01)

Bacterial strains expressing toluene and naphthalene dioxygenase were used to examine the sequence of reactions involved in the oxidation of 1,2-dihydronaphthalene. Toluene dioxygenase of Pseudomonas putida F39/D oxidizes 1,2-dihydronaphthalene to (+)-cis-(1S,2R)-dihydroxy-1,2,3,4-tetrahydronaphthalene, (+)-(1R)-hydroxy-1,2-dihydronaphthalene, and (+)-cis-(1R,2S)-dihydroxy-1,2-dihydronaphthalene. In contrast, naphthalene dioxygenase of Pseudomonas

Initial reactions in the oxidation of 1,2-dihydronaphthalene by Sphingomonas yanoikuyae strains.

S L Eaton et al.

Applied and environmental microbiology, 62(12), 4388-4394 (1996-12-01)

The substrate oxidation profiles of Sphingomonas yanoikuyae B1 biphenyl-2,3-dioxygenase and cis-biphenyl dihydrodiol dehydrogenase activities were examined with 1,2-dihydronaphthalene and various cis-diols as substrates. m-Xylene-induced cells of strain B1 oxidized 1,2-dihydronaphthalene to (-)-(1R,2S)-cis-1,2-dihydroxy-1,2-3,4-tetrahydronaphthalene as the major product (73% relative yield). Small

Asymmetric epoxidation using a singly-bound supported Katsuki-type (salen)Mn complex.

Keith Smith et al.

Chemical communications (Cambridge, England), (8)(8), 886-887 (2002-07-19)

We have successfully prepared an unsymmetrical analogue of a Katsuki-type salen ligand having a single hydroxyalkyl group at its 6-position, and also its Mn(III) complex; attachment of the complex to a polymer gives a highly enantioselective and recoverable catalyst for

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货号	GTIN
D105937-1G	04061837709111
D105937-25G	04061837709128
D105937-10G	04061833558447