Hydrocinchonidine
Based on 1 Customer Validation
Hydrocinchonidine is an alkaloid that can be used as a chiral base in the 1,3-dipolar cycloaddition reactions of alkenes and azomethine ylides using silver fluoride. Hydrocinchonidine can also be used to synthesize molecules withoptically active quaternary centers via the aza-Henry reaction.
연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.
- CAS No.: 485-64-3
- 화학식: C19H24N2O
- 분자량:296.41
-
보관:
4°C, protect from light, stored under nitrogen
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light, stored under nitrogen)
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
-
Biological Activity
-
Chemical Information
- 순도&문서
- References
-
Help & FAQs
Biological Activity
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| Huh-7 | CC50 |
>7.91 μM
Compound: GNF-Pf-1324
|
NOVARTIS: Cytotoxicity against human hepatocellular carcinoma cell line (Huh7)
NOVARTIS: Cytotoxicity against human hepatocellular carcinoma cell line (Huh7)
|
[PMID: 18579783] |
| Huh-7 | CC50 |
7.91 μM
Compound: GNF-Pf-1324
|
NOVARTIS: Cytotoxicity against human hepatocellular carcinoma cell line (Huh7)
NOVARTIS: Cytotoxicity against human hepatocellular carcinoma cell line (Huh7)
|
[PMID: 18579783] |
Chemical Information
-
CAS No. 485-64-3
-
Appearance Powder
-
분자량 296.41
-
화학식 C19H24N2O
-
Color White to off-white
-
SMILES
O[C@H](C1=CC=NC2=C1C=CC=C2)[C@@]3([H])[N@@](CC4)C[C@H](CC)[C@]4([H])C3
-
선적
Room temperature in continental US; may vary elsewhere.
-
보관
4°C, protect from light, stored under nitrogen
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light, stored under nitrogen)
순도&문서
-
Data Sheet (276 KB)
-
SDS (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
-
Handling Instructions (2659 KB)
References
[1]. Alemparte C, et al., A convenient procedure for the catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides and alkenes. Org Lett. 2005 Oct 13;7(21):4569-72. [Content Brief]
[2]. Knudsen KR, et al., A chiral molecular recognition approach to the formation of optically active quaternary centres in aza-Henry reactions. Org Biomol Chem. 2005 Apr 21;3(8):1362-4. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Hydrocinchonidine Related Classifications
HY-W035708 Related Classifications
Powered by Bioz