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Merck
CN

258563

2-甲基戊醛

98%

别名:

2-甲基正戊醛

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线性分子式:
CH3CH2CH2CH(CH3)CHO
化学文摘社编号:
分子量:
100.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-605-2
Beilstein/REAXYS Number:
1739423
MDL number:
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产品名称

2-甲基戊醛, 98%

InChI key

FTZILAQGHINQQR-UHFFFAOYSA-N

InChI

1S/C6H12O/c1-3-4-6(2)5-7/h5-6H,3-4H2,1-2H3

SMILES string

CCCC(C)C=O

vapor density

3.45 (vs air)

assay

98%

form

liquid

autoignition temp.

390 °F

refractive index

n20/D 1.401 (lit.)

bp

119-120 °C (lit.)

density

0.808 g/mL at 25 °C (lit.)

functional group

aldehyde

Quality Level

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General description

2-甲基戊醛与丙醛形成2,4-二甲基庚-2-烯醛的交叉羟醛缩合反应已有研究。用叠氮基三甲基硅烷和铬酐在CH2Cl2中氧化2-甲基戊醛已有研究

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 1

flash_point_f

60.8 °F - closed cup

flash_point_c

16 °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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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Oxidation of aldehydes to acyl azides by chromic anhydride-azidotrimethylsilane.
Lee JG and Kwak KH.
Tetrahedron Letters, 33(22), 3165-3166 (1992)
Valentina Innamorato et al.
Food chemistry, 315, 126247-126247 (2020-02-02)
Three non-targeted methods, i.e. 1H NMR, LC-HRMS, and HS-SPME/MS-eNose, combined with chemometrics, were used to classify two table grape cultivars (Italia and Victoria) based on five quality levels (5, 4, 3, 2, 1). Grapes at marketable quality levels (5, 4
Christian P Mehnert et al.
Chemical communications (Cambridge, England), (15), 1610-1611 (2002-08-13)
C9-aldehyde has been prepared via aldol condensation reactions in ionic liquid media; catalyst investigation showed enhanced product selectivity for the desired aldehyde in ionic liquid media than in conventional solvent systems.
Sajjad Ahmad et al.
Drug design, development and therapy, 15, 1299-1313 (2021-04-02)
Organocatalytic asymmetric Michael addition is a strong approach for C-C bond formation. The objective of the study is to design molecules by exploiting the efficiency of Michael Adducts. We proceeded with the synthesis of Michael adducts by tailoring the substitution

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