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5-carboxamidotryptamine maleate salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 118202-69-0 Structure
  • Basic information

    1. Product Name: 5-carboxamidotryptamine maleate salt
    2. Synonyms: 5-carboxamidotryptamine maleate salt
    3. CAS NO:118202-69-0
    4. Molecular Formula: C11H13N3O.C4H4O4
    5. Molecular Weight: 319.315
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 118202-69-0.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. CAS DataBase Reference: 5-carboxamidotryptamine maleate salt(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-carboxamidotryptamine maleate salt(118202-69-0)
    11. EPA Substance Registry System: 5-carboxamidotryptamine maleate salt(118202-69-0)
  • 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: 118202-69-0(Hazardous Substances Data)

118202-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118202-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,2,0 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 118202-69:
(8*1)+(7*1)+(6*8)+(5*2)+(4*0)+(3*2)+(2*6)+(1*9)=100
100 % 10 = 0
So 118202-69-0 is a valid CAS Registry Number.

118202-69-0Downstream Products

118202-69-0Relevant articles and documents

Indole compounds and use thereof

-

, (2008/06/13)

Compounds are disclosed of general formula (I): STR1 wherein R1 and R2 each independently represents a hydrogen atom, or an aryl, aralkyl, cycloalkyl, fluoroalkyl or alkyl group, which alkyl group is optionally substituted by an alkenyl group or by a group -OR7 or by STR2 where R7 and R8 each independently represents a hydrogen atom, an alkyl, aryl or aralkyl group; or R1 and R2 together with the nitrogen atom to which they are attached form a saturated monocyclic 5 to 7 membered ring which may contain a further hetero function (viz--O--, --NH or STR3 R3 and R4 have the same meanings as R1 and R2 and may together form an aralkylidene group; R5 represents a hydrogen atom or an alkyl or aralkyl group; R6 represents a hydrogen atom or an aryl or C1 -C3 alkyl group; Alk represents an C1 -C4 alkylene group optionally substituted at one or more of its carbon atoms by one to three C1 -C3 alkyl groups; and X represents an oxygen or sulphur atom, and its physiologically acceptable salts, hydrates and bioprecursors. The indoles (I) may be prepared by combinations of reactions to introduce the desired substituents into suitable intermediates either before or after cyclization to form the indole nucleus. The compounds have selective actions on blood vessels and, in particular exhibit antihypertensive properties. They may be formulated in conventional manner as pharmaceutical compositions.

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