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Merck
CN

150045

2,4-二甲基-3-戊醇

99%

别名:

二异丙基甲醇

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关于此项目

线性分子式:
(CH3)2CHCH(OH)CH(CH3)2
化学文摘社编号:
分子量:
116.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-993-7
Beilstein/REAXYS Number:
1731593
MDL number:
Assay:
99%
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产品名称

2,4-二甲基-3-戊醇, 99%

InChI key

BAYAKMPRFGNNFW-UHFFFAOYSA-N

InChI

1S/C7H16O/c1-5(2)7(8)6(3)4/h5-8H,1-4H3

SMILES string

CC(C)C(O)C(C)C

assay

99%

refractive index

n20/D 1.425 (lit.)

bp

139-140 °C (lit.)

density

0.829 g/mL at 25 °C (lit.)

functional group

hydroxyl

Quality Level

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Application

2,4-二甲基-3-戊醇用作与 2-取代丙烯酸酯衍生物的非对映选择性偶联的质子源。它用于 1,1′-(1,3-亚苯基)二乙醇(1,3-二醇)和己二酸二异丙酯的聚合反应

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

98.6 °F - closed cup

flash_point_c

37 °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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Liping Wang et al.
Pesticide biochemistry and physiology, 139, 46-52 (2017-06-10)
Camptothecin (CPT), a quinolone alkaloid extracted from Camptotheca acuminata Decne, exhibits potential insecticidal activities against various insect species. Our previous studies have showed that CPT induced apoptosis in Spodoptera exigua Hübner cell line and inhibited the relaxation activity of topoisomerase
Bart A C van As et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(29), 8325-8332 (2007-07-31)
The well-known dynamic kinetic resolution of secondary alcohols and esters was extended to secondary diols and diesters to afford chiral polyesters. This process is an example of iterative tandem catalysis (ITC), a polymerization method where the concurrent action of two
Hegui Gong et al.
Organic letters, 11(4), 879-882 (2009-01-28)
A mild, stereoselective method for the Ni-catalyzed synthesis of alpha-C-alkylglycosides is reported. This approach entails the reductive coupling of glycosyl bromides with activated alkenes at room temperature, with low alkene loading as an important feature. Diastereoselective coupling with 2-substituted acrylate

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