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Merck
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Key Documents

277681

Sigma-Aldrich

3-Methyl-3-oxetanemethanol

98%

동의어(들):

3-Hydroxymethyl-3-methyl-oxetane

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About This Item

실험식(Hill 표기법):
C5H10O2
CAS Number:
Molecular Weight:
102.13
Beilstein:
102773
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

98%

형태

liquid

refractive index

n20/D 1.446 (lit.)

bp

80 °C/40 mmHg (lit.)

density

1.024 g/mL at 25 °C (lit.)

저장 온도

2-8°C

SMILES string

CC1(CO)COC1

InChI

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

InChI key

NLQMSBJFLQPLIJ-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

3-Methyl-3-oxetanemethanol has been used in the preparation of:
  • star-shaped copolymer consisting of a hyperbranched poly(3-methyl-3-oxetanemethanol) core and polytetrahydrofuran arms
  • pyridyl disulfide-functionalized cyclic carbonate monomer, required for the synthesis of of functional poly(ε-caprolactone) containing pendant pyridyl disulphide groups
  • δ-lactams

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

206.6 °F - closed cup

Flash Point (°C)

97 °C - closed cup

개인 보호 장비

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


시험 성적서(COA)

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이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

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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