추천 제품
Grade
produced by BASF
vapor pressure
0.5 mmHg ( 20 °C)
분석
≥99.0% (GC)
≥99.0%
양식
liquid
광학 순도
enantiomeric excess: ≥98.0%
refractive index
n20/D 1.526 (lit.)
bp
187-189 °C (lit.)
density
0.952 g/mL at 20 °C (lit.)
작용기
amine
phenyl
SMILES string
C[C@@H](N)c1ccccc1
InChI
1S/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3/t7-/m1/s1
InChI key
RQEUFEKYXDPUSK-SSDOTTSWSA-N
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일반 설명
(R)-(+)-α-Methylbenzylamine is a chiral amine.
애플리케이션
(R)-(+)-α-Methylbenzylamine may be used as a substrate to synthesize:
- (S)-α-amino phosphonates
- N-{(S)-[cyclohexan-(S)-2-ol]}-(R)-α-methylbenzyl amine and N-{(R)-[cyclohexan-(R)-2-ol]}-(R)-α-methylbenzyl amine
- R-α-aminonitriles
법적 정보
ChiPros is a registered trademark of BASF SE
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 1
Flash Point (°F)
158.0 °F - closed cup
Flash Point (°C)
70 °C - closed cup
이미 열람한 고객
New enantiomerically pure aminoalcohols from (R)-a-methylbenzylamine and cyclohexene oxide.
Barbaro P, et al.
Tetrahedron Asymmetry, 7(3), 843-850 (1996)
Lithium perchlorate/diethylether catalyzed aminophosphonation of aldehydes.
Heydari A, et al.
Tetrahedron Letters, 39(37), 6729-6732 (1998)
ChiPros Chiral Amines
Aldrich Chemfiles, 11(1) null
Alejandra León et al.
Journal of natural products, 75(5), 859-864 (2012-05-12)
The enantiomeric lactams (-)-8, (+)-8, (+)-9, and (-)-9 were formed by the reaction of the dimeric phthalide rac-tokinolide B (rac-3) with (R)-(+)-α-methylbenzylamine and (S)-(-)-α-methylbenzylamine. The absolute configurations of compounds 8 and 9 were assigned by experimental and theoretically calculated electronic
Paul E Harrington et al.
Current medicinal chemistry, 14(28), 3027-3034 (2008-01-29)
The calcium sensing receptor (CaR) is a G protein-coupled receptor (GPCR) that plays a fundamental role in serum calcium homeostasis. The CaR is expressed on the chief cells of the parathyroid gland and is responsible for controlling the secretion of
문서
Chiral amines play an important role in stereoselective organic synthesis. They are used directly as resolving agents, building blocks, or chiral auxiliaries.
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