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Merck
모든 사진(1)

문서

248533

Sigma-Aldrich

5-Norbornene-2-methanol

98%, mixture of endo and exo

동의어(들):

2-(Hydroxymethyl)bicyclo[2.2.1]hept-5-ene, 2-Hydroxymethyl-5-norbornene, 2-Norbornen-5-methanol, 5-(Hydroxymethyl)bicyclo[2.2.1]hept-2-ene, 5-Hydroxymethyl-2-norbornene, Bicyclo[2.2.1]hept-5-en-2-ylmethanol, Norbornene-5-methyl alcohol, [Bicyclo[2.2.1]hept-5-en-2-yl]methanol

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About This Item

실험식(Hill 표기법):
C8H12O
CAS Number:
Molecular Weight:
124.18
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

98%

형태

liquid

refractive index

n20/D 1.500 (lit.)

bp

97 °C/20 mmHg (lit.)

density

1.027 g/mL at 25 °C (lit.)

SMILES string

OCC1C[C@@H]2C[C@H]1C=C2

InChI

1S/C8H12O/c9-5-8-4-6-1-2-7(8)3-6/h1-2,6-9H,3-5H2/t6-,7+,8?/m0/s1

InChI key

LUMNWCHHXDUKFI-KJFJCRTCSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

Co-polymerization of 5-norbornene-2-methanol with ethylene using heterogeneous silica supported catalysts has been reported.

애플리케이션

5-Norbornene-2-methanol has been used in the preparation of:
  • 4-(norborn-2-ene-5-ylmethyleneoxy)-2,2′:6′,2′′-terpyridine
  • 5- {[(3,5-di-t-butyl-4-hydroxy-benzoyl)oxy]methyl}-2-norbornene (BHBN)

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

188.6 °F - closed cup

Flash Point (°C)

87 °C - closed cup

개인 보호 장비

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


시험 성적서(COA)

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Synthesis of a polynorbornene containing 3, 5-di-TERT-butyl-4-hydroxybenzoyl group.
Tienkopatchev MA, et al.
Polymer Bull., 34(4), 385-391 (1995)
Access to heterogeneous atom-transfer radical polymerization (ATRP) catalysts based on dipyridylamine and terpyridine via ring-opening metathesis polymerization (ROMP).
Kroll R, et al.
Macromolecular Chemistry and Physics, 202(5), 645-653 (2001)
Homogeneous and heterogeneous metallocene/MAO-catalyzed polymerization of functionalized olefins.
Goretzki R and Fink G.
Macromolecular Chemistry and Physics, 200(4), 881-886 (1999)
Zhen Zhang et al.
Polymers, 12(4) (2020-04-16)
Injectable, covalently cross-linked hydrogels have been widely investigated in drug delivery systems due to their superior mechanical properties and long-term stability. Conventional covalently cross-linked hydrogels are formed by chemical reactions that may interfere with natural biochemical processes. In this work

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