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Merck

277681

3-甲基-3-羟甲基氧杂环丁烷

98%

同義詞:

3-羟甲基-3-甲基氧杂环丁烷

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關於此項目

經驗公式(希爾表示法):
C5H10O2
CAS 編號:
分子量::
102.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
102773

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產品名稱

3-甲基-3-羟甲基氧杂环丁烷, 98%

InChI

1S/C5H10O2/c1-5(2-6)3-7-4-5/h6H,2-4H2,1H3

SMILES string

CC1(CO)COC1

InChI key

NLQMSBJFLQPLIJ-UHFFFAOYSA-N

assay

98%

form

liquid

refractive index

n20/D 1.446 (lit.)

bp

80 °C/40 mmHg (lit.)

density

1.024 g/mL at 25 °C (lit.)

functional group

ether
hydroxyl

storage temp.

2-8°C

Quality Level

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本產品
745715745693591653
assay

98%

assay

97%

assay

97%

assay

98%

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

100

bp

80 °C/40 mmHg (lit.)

bp

-

bp

-

bp

-

density

1.024 g/mL at 25 °C (lit.)

density

1.092 g/mL at 25 °C

density

1.014 g/mL at 25 °C

density

-

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

-

refractive index

n20/D 1.446 (lit.)

refractive index

n20/D 1.450

refractive index

n20/D 1.458

refractive index

-

Application

3-甲基-3-氧杂依那西普乙醇已用于制备:
  • 由超支化聚(3-甲基-3-氧杂乙二胺乙醇)核心和聚四氢呋喃臂组成的星形共聚物[1]
  • 用于合成官能性聚(ε-己内酯)含有侧基吡啶基二硫化物基团的吡啶基二硫键官能化的环状碳酸酯单体[2]
  • δ -内酰胺类[3]

存儲類別/等級

10 - Combustible liquids

wgk

WGK 3

flash_point_f

206.6 °F - closed cup

flash_point_c

97 °C - closed cup

ppe

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


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分析證明 (COA)

Lot/Batch Number

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存取文件庫

Synthesis of a Star-Shaped Copolymer with a Hyperbranched Poly (3-methyl-3-oxetanemethanol) Core and Tetrahydrofuran Arms by One-Pot Copolymerization.
Hou J and Yan D.
Macromolecular Rapid Communications, 23(8), 456-459 (2002)
Functional poly (e-caprolactone) s via copolymerization of e-caprolactone and pyridyl disulfide-containing cyclic carbonate: controlled synthesis and facile access to reduction-sensitive biodegradable graft copolymer micelles.
Chen W, et al.
Macromolecules, 46(3), 699-707 (2013)
Bhooma Raghavan et al.
The Journal of organic chemistry, 71(5), 2151-2154 (2006-02-25)
A concise, stereoselective synthesis of alpha-substituted gamma-lactams is reported. gamma-Lactam scaffolds 2 and 3, possessing an Evans' chiral auxiliary and two types of N substituents, were successfully alkylated with different electrophiles to give alpha-substituted gamma-lactams with reasonable diastereoselectivities. The use
Gintare Krucaite et al.
Molecules (Basel, Switzerland), 26(7) (2021-04-04)
A group of polyethers containing electroactive pendent 4,7-diarylfluorene chromophores have been prepared by the multi-step synthetic route. Full characterization of their structures has been presented. The polymeric materials represent derivatives of high thermal stability with initial thermal degradation temperatures in

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