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Rugulovasine B is an alkaloid isomer derived from the cultures of Penicillium concavorugulosum. It exists as an amorphous solid that cannot be crystallized and has a specific optical rotation of [α]22436 + lAO (c 1.0, pyridine). Rugulovasine B can be converted into its corresponding dihydro derivative, which has a melting point of 222-5°C (dec.).

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  • 26909-34-2 Structure
  • Basic information

    1. Product Name: rugulovasine B
    2. Synonyms: rugulovasine B;RUGULOVASINB
    3. CAS NO:26909-34-2
    4. Molecular Formula: C16H16N2O2
    5. Molecular Weight: 268.31044
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 26909-34-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 550.3°Cat760mmHg
    3. Flash Point: 286.6°C
    4. Appearance: /
    5. Density: 1.32g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: rugulovasine B(CAS DataBase Reference)
    10. NIST Chemistry Reference: rugulovasine B(26909-34-2)
    11. EPA Substance Registry System: rugulovasine B(26909-34-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 26909-34-2(Hazardous Substances Data)

26909-34-2 Usage

Uses

Used in Pharmaceutical Industry:
Rugulovasine B is used as a pharmaceutical compound for its potential therapeutic applications. The expression is: rugulovasine B is used as a pharmaceutical compound for its potential therapeutic applications.
Used in Research and Development:
Rugulovasine B is used as a research compound for studying its chemical properties, structural characteristics, and possible interactions with other molecules. The expression is: rugulovasine B is used as a research compound for studying its chemical properties, structural characteristics, and possible interactions with other molecules.
Used in Drug Delivery Systems:
Rugulovasine B can be utilized in the development of novel drug delivery systems to enhance its applications and efficacy in various therapeutic areas. The expression is: rugulovasine B is used as a component in drug delivery systems for improving its delivery, bioavailability, and therapeutic outcomes.

References

Abe et al., Agr. Bioi. Chern., (Tokyo), 33,469 (1969) Abe et al., Nippon Nogeikagaku Kaishi, 43, 575 (1969) Yamatodani et al., A gr. Bioi. Chern., (Tokyo), 34, 485 (1970)

Check Digit Verification of cas no

The CAS Registry Mumber 26909-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,0 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 26909-34:
(7*2)+(6*6)+(5*9)+(4*0)+(3*9)+(2*3)+(1*4)=132
132 % 10 = 2
So 26909-34-2 is a valid CAS Registry Number.

26909-34-2SDS

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 rugulovasine B

1.2 Other means of identification

Product number -
Other names -

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:26909-34-2 SDS

26909-34-2Downstream Products

26909-34-2Relevant articles and documents

Applications of vinylogous Mannich reactions. Total syntheses of the Ergot alkaloids rugulovasines A and B and setoclavine

Liras,Lynch,Fryer,Vu,Martin

, p. 5918 - 5924 (2007/10/03)

Concise syntheses of the Ergot alkaloids rugulovasine A (3a), rugulovasine B (3b), and setoclavine (2) have been completed by strategies that feature inter- and intramolecular vinylogous Mannich reactions as the key steps. Thus, the first synthesis of 3a,

The Rugulovasines: Synthesis, Structure, and Interconversions

Rebek, J.,Shue, Y.-K.,Tai, D. F.

, p. 3540 - 3545 (2007/10/02)

Experimental details are provided for the synthesis of the rugulovasine alkaloids from tryptophan.Optically active rugulovasine A is prepared for the first time and details concerning its conformation, racemization, and isomerization to rugulovasine B are presented.

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