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Oxysophoridine is an alkaloid that has been isolated from Sophora alopecuroides L. It forms colorless needles when crystallized from Me2CO and has a specific rotation of [α]D-50.6° (c 0.555, EtOH). The alkaloid can be acetylated to form its O-acetate, which has a melting point of 148-147°C.

54809-74-4

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54809-74-4 Usage

Uses

Used in Pharmaceutical Industry:
Oxysophoridine is used as a pharmaceutical compound for its potential therapeutic properties. Its unique structure and properties make it a promising candidate for the development of new drugs and treatments.
Used in Chemical Research:
Oxysophoridine is used as a research compound in the field of chemistry, particularly in the study of alkaloids and their properties. Its isolation and characterization provide valuable insights into the chemical properties and potential applications of this class of compounds.
Used in Natural Product Chemistry:
Oxysophoridine is used as a natural product in the study of plant-derived compounds and their potential applications in various industries. Its isolation from Sophora alopecuroides L. highlights the importance of exploring natural sources for novel and bioactive compounds.

References

Monakhova et at., Khim. Prir. Soedin., 9,59 (1973)

Check Digit Verification of cas no

The CAS Registry Mumber 54809-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,0 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54809-74:
(7*5)+(6*4)+(5*8)+(4*0)+(3*9)+(2*7)+(1*4)=144
144 % 10 = 4
So 54809-74-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H24N2O2/c18-14-7-1-6-13-12-5-3-9-17(19)8-2-4-11(15(12)17)10-16(13)14/h11-13,15H,1-10H2/t11-,12-,13-,15+,17?/m1/s1

54809-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-matrine N-oxide

1.2 Other means of identification

Product number -
Other names OXYMATRINE

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:54809-74-4 SDS

54809-74-4Relevant academic research and scientific papers

Direct preparation of unprotected aminimides (R3N+-NH-) from natural aliphatic tertiary alkaloids (R3N) by [Mn(TDCPP)Cl]-catalysed: N -amination reaction

Che, Chi-Ming,Liu, Yungen,Xing, Fangrong,Zhang, Shilong

supporting information, p. 9102 - 9105 (2020/08/26)

A panel of natural aliphatic tertiary alkaloids (R3N) were directly converted to R3N+-NH- (without the need to prepare protected aminimides R3N+-NR′- followed by deprotection) by [Mn(TDCPP)Cl]-catalysed N-amination reaction, with O-(2,4-dinitrophenyl)hydroxylamine as the nitrogen source, in up to 98% yields under mild reaction conditions.

PROCESS FOR THE PURIFICATION OF SOPHORA ALKALOIDS

-

Page/Page column 10, (2009/10/22)

A method of purifying alkaloids extracted from plants of the Sophora genus (Sophora alkaloids), characterised in that the method comprises a purification step in which the Sophora alkaloids are placed on a macroporous absorption resin with an eluent comprising at least 40wt% water.

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