추천 제품
vapor density
5.24 (vs air)
Quality Level
vapor pressure
4 mmHg ( 70 °C)
분석
98%
양식
powder
광학 활성
[α]25/D +44.1°, c = 10 in ethanol
autoignition temp.
870 °F
expl. lim.
3.5 %
mp
179-181 °C (lit.)
작용기
ketone
SMILES string
C[C@@]1(CC2)C(C)(C)[C@H]2CC1=O
InChI
1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3/t7-,10+/m1/s1
InChI key
DSSYKIVIOFKYAU-XCBNKYQSSA-N
애플리케이션
(1R)-(+)-Camphor has been used as a standard during the enantioselective gas chromatography-mass spectrometry (GC-MS) analysis of the constituents of Achillea ligustica essential oil.
It may also be used to synthesize:
It may also be used to synthesize:
- {N,N′-bis[(1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl]-1,2-ethanediamine}, a C2-symmetrical diamine
- chiral oxazaborolidines
- (-)-(1R,2R)-1,2-dihydroxy-3,3-dimethylnorbornane
Chiral intermediate and auxiliary.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Sol. 2 - Skin Irrit. 2 - STOT SE 2 Inhalation
표적 기관
Lungs
Storage Class Code
4.1B - Flammable solid hazardous materials
WGK
WGK 1
Flash Point (°F)
147.2 °F - closed cup
Flash Point (°C)
64 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
Lot/Batch Number
이미 열람한 고객
Synthesis of C 2-symmetrical diamine based on (1R)-(+)-camphor and application to oxidative aryl coupling of naphthols.
Caselli A, et al.
Tetrahedron Asymmetry, 14(11), 1451-1454 (2003)
Synthetic Communications, 23, 437-437 (1993)
The Journal of Organic Chemistry, 56, 1185-1185 (1991)
Synthesis of homochiral 1, 2-diols from (-)-fenchone and (+)-camphor.
Martinez AG, et al.
Tetrahedron Asymmetry, 5(7), 1373-1376 (1994)
Asymmetric reduction of prochiral ketones using in situ generated oxazaborolidines derived from amino alcohols of (1R)-camphor as catalysts.
Santhi V and Rao JM
Tetrahedron Asymmetry, 11(17), 3553-3560 (2000)
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