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63785-22-8

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63785-22-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63785-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,8 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63785-22:
(7*6)+(6*3)+(5*7)+(4*8)+(3*5)+(2*2)+(1*2)=148
148 % 10 = 8
So 63785-22-8 is a valid CAS Registry Number.
InChI:InChI=1/C27H48N2O2/c1-15-11-23(31)25(29-14-15)16(2)24-22(30)13-21-19-6-5-17-12-18(28)7-9-26(17,3)20(19)8-10-27(21,24)4/h15-25,29-31H,5-14,28H2,1-4H3/t15-,16+,17+,18+,19-,20+,21+,22-,23+,24+,25-,26+,27+/m1/s1

63785-22-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3S,5R)-2-[(1S)-1-[(3S,5S,8R,9S,10S,13S,14S,16R,17R)-3-amino-16-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]ethyl]-5-methylpiperidin-3-ol

1.2 Other means of identification

Product number -
Other names 3-Piperidinol,2-[(3b,5a,16a,20S)-3-amino-16-hydroxypregnan-20-yl]-5-methyl-,(2R,3S,5R)-(9CI)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:63785-22-8 SDS

63785-22-8Upstream product

63785-22-8Relevant articles and documents

Studies on Indian Medicinal Plants. Part 77. Structure and Stereochemistry of Some New Steroidal Alkaloids from Solanum pseudocapsicum and Solanum giganteum by Nuclear Magnetic Resonance Spectroscopy

Chakravarty, Ajit K.,Das, Binayak,Ali, Esahak,Pakrashi, Satyesh C.

, p. 467 - 474 (2007/10/02)

Three new stereoisomeric steroidal alkaloids, viz. solacapine (6), episolacapine (11), and isosolacapine (13), along with another hitherto unreported base, O-methylsolanocapsine (3), have been isolated from the arboreal part of Solanum pseudocapsicum Linn.They have been characterised as (20S, 22R, 23S, 25R)-, (20S, 22R, 23R, 25R)-, and (20S, 22S, 23S, 25R)-3β-amino-16α,23-hydroxy-22,26-epimino-5α-cholestanes, respectively, primarily based on 1H and 13C n.m.r. spectra.The structures of (3), (6), and (11) could be confirmed by correlation with solanocapsine (1).Isosolacapsine (13) turned out to be the first 22,26-epiminocholestane derivative encountered in nature with 22βN stereochemistry.A diagnostic down-field shift of the C-22 resonance frequency in the 13C n.m.r. spectra of 22βN-22,26-epiminocholestanes by ca. 3 p.p.m. relative to those of the corresponding 22αN-isomers has been observed.The C-25 stereochemistry of solanogantamine (28) and isosolanogantamine (29), the stereoisomeric 3-amino solanidanes isolated from Solanum gigantem Jacq., has also been established.

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