219576
(1S)-(+)-10-Camphorsulfonyl chloride
97%
동의어(들):
(+)-Camphor-10-sulfonyl chloride, (1S)-Camphor-10-sulfonic acid chloride
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
실험식(Hill 표기법):
C10H15ClO3S
CAS Number:
Molecular Weight:
250.74
Beilstein:
3205974
EC Number:
MDL number:
UNSPSC 코드:
12352115
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
97%
형태
solid
mp
65-67 °C (lit.)
SMILES string
[H][C@@]12CC[C@@](CS(Cl)(=O)=O)(C(=O)C1)C2(C)C
InChI
1S/C10H15ClO3S/c1-9(2)7-3-4-10(9,8(12)5-7)6-15(11,13)14/h7H,3-6H2,1-2H3/t7-,10-/m1/s1
InChI key
BGABKEVTHIJBIW-GMSGAONNSA-N
애플리케이션
Chiral resolving agent. Used in the synthesis of nonpeptide oxytocin antagonists.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
B E Evans et al.
Journal of medicinal chemistry, 35(21), 3919-3927 (1992-10-16)
The first nonpeptide antagonists of the neurohypophyseal hormone, oxytocin (OT) are described. Derivatives of the spiroindenepiperidine ring system, these compounds include L-366,509, an orally bioavailable OT antagonist with good in vivo duration. The potential use of these agents for treatment
Synthesis, 947-947 (1992)
T Jira et al.
Die Pharmazie, 48(11), 829-833 (1993-11-01)
Investigations on direct separation by RP-HPLC of selected enantiomeric beta-adrenergic active agents are described. R- and S-1-phenylethylisocyanate (PEIC) as well as (1S)-(+)-campher-10-sulfonylchloride (CSC) are used for the derivatization of the compounds. Correlations between chromatographic data and various influences (pH, temperature
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