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13365

N,N-二甲基苄胺

Name: <I>N</I>,<I>N</I>-二甲基苄胺
Brand: SIGMA

≥99.5% (GC)

别名:

N-苄基二甲胺, BDMA, DMBA

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关于此项目

线性分子式:

C₆H₅CH₂N(CH₃)₂

化学文摘社编号:

103-83-3

分子量:

135.21

UNSPSC Code:

12352200

NACRES:

NA.26

PubChem Substance ID:

57647074

EC Number:

203-149-1

Beilstein/REAXYS Number:

1099620

MDL number:

MFCD00008329

Assay:

≥99.5% (GC)

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属性

assay

≥99.5% (GC)

refractive index

n20/D 1.501 (lit.), n20/D 1.502

bp

183-184 °C/765 mmHg (lit.)

mp

−75 °C (lit.)

solubility

H₂O: soluble

density

0.9 g/mL at 25 °C (lit.)

SMILES string

CN(C)Cc1ccccc1

InChI

1S/C9H13N/c1-10(2)8-9-6-4-3-5-7-9/h3-7H,8H2,1-2H3

InChI key

XXBDWLFCJWSEKW-UHFFFAOYSA-N

说明

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pictograms

GHS02,GHS06,GHS05,GHS09

signalword

Danger

hcodes

H226,H301 + H331,H312,H314,H411

pcodes

P210 - P273 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

存储类别

3 - Flammable liquids

wgk

WGK 2

flash_point_f

134.6 °F - closed cup

flash_point_c

57 °C - closed cup

ppe

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

法规信息

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Synthesis of optically active organoantimony compounds having an (S)-alpha-methylbenzyldimethylamine group and its evaluation for asymmetric reaction.

Shuji Yasuike et al.

Chemical & pharmaceutical bulletin, 50(10), 1404-1406 (2002-10-10)

Novel, enantiomerically pure organoantimony compounds having a C-chiral amine moiety, (S)-(alpha-methyl-2-di-p-tolylstibanobenzyl)dimethylamine [AMSb] (2) and its (eta(6)-arene)chromium complex [AMSb-Cr(CO)(3)] (4), were prepared from common (S)-(alpha-methylbenzyl)dimethylamine (1) via its ortho-lithiated intermediates in short steps. The catalytic activity and enantioselectivity of the ligands

Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: NMR desymmetrization of meso compounds.

Y Kobayashi et al.

Organic letters, 3(14), 2253-2255 (2001-07-07)

[structure: see text] Examples of (13)C NMR desymmetrization of meso compounds are presented. On analysis of the NMR profiles of 1,3-diols, the additivity is recognized to predict the NMR profiles of 1,3,5-tirols.

Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: scope and limitation.

N Hayashi et al.

Organic letters, 3(14), 2249-2252 (2001-07-07)

[structure: see text] Three additional NMR databases, 1-3, in a chiral solvent are presented. The C.21-C.38 portion of oasomycin A is used to demonstrate the scope and limitation of the universal NMR database approach in a chiral solvent for assignment

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全球贸易项目编号

货号	GTIN
13365-50ML-F	04061838169020

主要文件

N,N-二甲基苄胺

≥99.5% (GC)

选择尺寸

关于此项目

assay

refractive index

bp

mp

solubility

density

SMILES string

InChI

InChI key

Still not finding the right product?

安全信息

pictograms

signalword

hcodes

pcodes

Hazard Classifications

存储类别

wgk

flash_point_f

flash_point_c

ppe

法规信息

文件

分析证书(COA)

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