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methyl {(2S,3R,E)-3-[2-(benzyloxy)ethyl]-6-hydroxy-2-(2-methoxyphenyl)hex-4-en-1-yl}carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1630067-78-5 Structure
  • Basic information

    1. Product Name: methyl {(2S,3R,E)-3-[2-(benzyloxy)ethyl]-6-hydroxy-2-(2-methoxyphenyl)hex-4-en-1-yl}carbamate
    2. Synonyms: methyl {(2S,3R,E)-3-[2-(benzyloxy)ethyl]-6-hydroxy-2-(2-methoxyphenyl)hex-4-en-1-yl}carbamate
    3. CAS NO:1630067-78-5
    4. Molecular Formula:
    5. Molecular Weight: 413.514
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1630067-78-5.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: methyl {(2S,3R,E)-3-[2-(benzyloxy)ethyl]-6-hydroxy-2-(2-methoxyphenyl)hex-4-en-1-yl}carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl {(2S,3R,E)-3-[2-(benzyloxy)ethyl]-6-hydroxy-2-(2-methoxyphenyl)hex-4-en-1-yl}carbamate(1630067-78-5)
    11. EPA Substance Registry System: methyl {(2S,3R,E)-3-[2-(benzyloxy)ethyl]-6-hydroxy-2-(2-methoxyphenyl)hex-4-en-1-yl}carbamate(1630067-78-5)
  • 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: 1630067-78-5(Hazardous Substances Data)

1630067-78-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1630067-78-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,3,0,0,6 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1630067-78:
(9*1)+(8*6)+(7*3)+(6*0)+(5*0)+(4*6)+(3*7)+(2*7)+(1*8)=145
145 % 10 = 5
So 1630067-78-5 is a valid CAS Registry Number.

1630067-78-5Relevant articles and documents

A unified strategy for kainoid synthesis

Fujii, Masaya,Yokoshima, Satoshi,Fukuyama, Tohru

, p. 4823 - 4836 (2014/08/05)

A unified strategy for kainoid synthesis was developed. The key features of the strategy involve a Claisen-Ireland rearrangement to construct the contiguous stereogenic centers and a palladium-catalyzed formation of the pyrrolidine ring with complete stereoselectivity. The present protocol has enabled rapid access to a wide range of kainoids with diverse types of substituents (alkenyl, aryl, and alkyl groups) at the 4-position of the pyrrolidine ring, starting from the common intermediate and appropriate acetic acid derivatives. To test the generality of the strategy, we have accomplished the syntheses of kainic acid, o-methoxyphenyl derivative (MFPA), and a novel cyclopropyl derivative (CPKA), using 3-methylbut-3-enoic acid, 2-(2-methoxyphenyl)acetic acid, and 2-cyclopropylacetic acid, respectively.

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