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140387-89-9

S-(-)-LISURIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 140387-89-9 Structure

  • Basic information

    1. Product Name: S-(-)-LISURIDE
    2. Synonyms: S-(-)-LISURIDE;LISURIDE;DL-Lisuride;Urea, N'-[(8a)-()-9,10-didehydro-6-methylergolin-8-yl]-N,N-diethyl- (9CI);3-[(6aR,9S)-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-yl]-1,1-diethylurea
    3. CAS NO:140387-89-9
    4. Molecular Formula: C20H26N4O
    5. Molecular Weight: 338.45
    6. EINECS: N/A
    7. Product Categories: API
    8. Mol File: 140387-89-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: pKa 7.29(H2O,t =37,I=0.15) (Uncertain)
    10. CAS DataBase Reference: S-(-)-LISURIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: S-(-)-LISURIDE(140387-89-9)
    12. EPA Substance Registry System: S-(-)-LISURIDE(140387-89-9)

  • 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: 140387-89-9(Hazardous Substances Data)

140387-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140387-89-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,3,8 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 140387-89:
(8*1)+(7*4)+(6*0)+(5*3)+(4*8)+(3*7)+(2*8)+(1*9)=129
129 % 10 = 9
So 140387-89-9 is a valid CAS Registry Number.

140387-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name S-(-)-LISURIDE

1.2 Other means of identification

Product number -
Other names Urea,N'-[(8a)-()-9,10-didehydro-6-methylergolin-8-yl]-N,N-diethyl-(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:140387-89-9 SDS

140387-89-9Upstream product

140387-89-9Relevant articles and documents

Use of 1-(8-alpha-ergolinyl)-3,3-diethyl urea derivatives in the treatment of endometritis

-

, (2008/06/13)

A composition for the treatment of endometritis in mammalian females which comprises as the physiologically active component a 1-(8alpha-ergolinyl)-3,3-diethylurea of the general formula I in which R1 represents an alkyl group containing from 1 to 3 carbon atoms, R2 represents a hydrogen atom or an alkyl group containing from 1 to 3 carbon atoms and either X stands for a hydrogen atom or both of them form jointly an additional bond between carbon atoms in positions 9 and 10, or a pharmaceutically acceptable acid addition salt thereof. The subject composition of the invention is suitable for treating acute puerperal inflammations and chronic endometritis in mammalian females, especially farm animal females, e.g. cows.

SOLVOLYSIS OF SOME 1-(8α-ERGOLINYL)-3,3-DIETHYLUREAS AND THEIR SALTS

Cerny, Antonin,Benes, Jan,Vachek, Jaroslav,Pesak, Milan,Stuchlik, Josef,et al.

, p. 1331 - 1339 (2007/10/02)

Nine salts of 1-(8α-ergolinyl)-3,3-diethylurea (II) were prepared and their solubility in water and the stability of the aqueous solutions at 60 and 100 deg C were studied.The main product of hydrolysis is 6-methyl-8α-aminoergoline IV.The urethan VII is formed in the ethanolic solution.Both decomposition products are also formed under long-term storage at +5 deg C.The course of hydrolysis of N-propyl homologue III is similar.The decomposition of 9,10-didehydro derivative I is much slower under the conditions used.

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