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I1804

茚满

Name: 茚满
Brand: ALDRICH

95%

别名:

二氢化茚

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关于此项目

经验公式（希尔记法）:

C₉H₁₀

化学文摘社编号:

496-11-7

分子量:

118.18

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24895949

EC Number:

207-814-7

Beilstein/REAXYS Number:

1904376

MDL number:

MFCD00003795

Assay:

95%

Form:

liquid

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属性

Quality Level

100

assay

95%

form

liquid

refractive index

n20/D 1.537 (lit.)

bp

176 °C (lit.)

mp

−51 °C (lit.)

density

0.965 g/mL at 25 °C (lit.)

SMILES string

C1Cc2ccccc2C1

InChI

1S/C9H10/c1-2-5-9-7-3-6-8(9)4-1/h1-2,4-5H,3,6-7H2

InChI key

PQNFLJBBNBOBRQ-UHFFFAOYSA-N

Gene Information

human ... CYP1A2(1544)

说明

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pictograms

GHS02,GHS08

signalword

Danger

hcodes

H226,H304

pcodes

P210 - P233 - P240 - P241 - P301 + P310 - P331

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 3

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

129.2 °F - closed cup

flash_point_c

54 °C - closed cup

ppe

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

法规信息

危险化学品

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Asymmetric hydrogenation of ketones catalyzed by a ruthenium(II)-indan-ambox complex.

Wei Li et al.

Chemical communications (Cambridge, England), 46(22), 3979-3981 (2010-04-22)

(S,R)-Indan-ambox ligand and its ruthenium(II) complex have been prepared and successfully applied to asymmetric hydrogenation of prochiral simple ketones. A wide range of unfunctionalized ketones are reduced by Ru(II)-indan-ambox catalyst with excellent enantioselectivities (up to 97% ee).

Highly efficient biocatalytic resolution of cis- and trans-3-aminoindan-1-ol: syntheses of enantiopure orthogonally protected cis- and trans-indane-1,3-diamine.

Mónica López-García et al.

Chemistry (Weinheim an der Bergstrasse, Germany), 10(12), 3006-3014 (2004-06-24)

The efficient chemoenzymatic synthesis of enantiopure 1,3-difunctionalized indane derivatives has been achieved. The corresponding cis and trans N-protected amino alcohols were successfully resolved by acetylation using lipase B, which is a biocatalyst isolated from Candida antarctica. All the possible isomers

A new NF-kappaB inhibitor attenuates a TH1 type immune response in a murine model.

Kenji Kabashima et al.

FEBS letters, 578(1-2), 36-40 (2004-12-08)

Nuclear factor kappa B (NF-kappaB) plays a wide variety of pathophysiological roles and modulation of its pathway can be a good novel drug target. Here, we found that our recently synthesized NF-kappaB inhibitor attenuated an ovalbumin-specific delayed-type hypersensitivity response in

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全球贸易项目编号

货号	GTIN
I1804-500ML	04061838124180
I1804-100ML	04061833848128