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CAS

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127906-09-6

[2-(3-Methoxy-phenylsulfanyl)-benzyl]-dipropyl-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127906-09-6 Structure

  • Basic information

    1. Product Name: [2-(3-Methoxy-phenylsulfanyl)-benzyl]-dipropyl-amine
    2. Synonyms:
    3. CAS NO:127906-09-6
    4. Molecular Formula:
    5. Molecular Weight: 329.506
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127906-09-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: [2-(3-Methoxy-phenylsulfanyl)-benzyl]-dipropyl-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: [2-(3-Methoxy-phenylsulfanyl)-benzyl]-dipropyl-amine(127906-09-6)
    11. EPA Substance Registry System: [2-(3-Methoxy-phenylsulfanyl)-benzyl]-dipropyl-amine(127906-09-6)

  • 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: 127906-09-6(Hazardous Substances Data)

127906-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127906-09-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,9,0 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 127906-09:
(8*1)+(7*2)+(6*7)+(5*9)+(4*0)+(3*6)+(2*0)+(1*9)=136
136 % 10 = 6
So 127906-09-6 is a valid CAS Registry Number.

127906-09-6Downstream Products

127906-09-6Relevant articles and documents

POTENTIAL ANTIDEPRESSANTS: 2-(METHOXY- AND HYDROXY-PHENYLTHIO)BENZYLAMINES AS SELECTIVE INHIBITORS OF 5-HYDROXYTRYPTAMINE RE-UPTAKE IN THE BRAIN

Jilek, Jiri,Sindelar, Karel,Pomykacek, Josef,Kmonicek, Vojtech,Sedivy, Zdenek,et al.

, p. 3294 - 3338 (2007/10/02)

2-, 3- and 4-Methoxythiophenol, and 2,4-, 2,5- and 3,4-dimethoxythiophenol were transformed in two steps to the corresponding 2-(methoxyphenylthio)benzoyl chlorides XIII which were reacted with ammonia, methylamine, dimethylamine, diethylamine, dipropylamine, and di(2-propyl)amine to give the amides XIV-XIX.These were reduced mostly with lithium aluminium hydride to the amines II-VII.These methoxylated amines were demethylated mostly either by heating with pyridine hydrochloride or by treatment with boron tribromide.Some of the 2-(methoxy- and hydroxy-phenylthio)benzylamines prepared, especially compounds II, III, XXI, and XXII, indicated properties of potential antidepressants being highly active and selective inhibitors of 5-hydroxytryptamine re-uptake in the brain structures and having the typical antireserpine activity.The most interesting compound of the series is XXIb (hydrogen maleate VUFB-15 468) which is undergoing preclinical studies.On the basis of its structure, some further compounds (XXVII-XXIX, XXXIX-XLI) were prepared by various methods.

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