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(+/-) methyl (4,5)-anti-5-hydroxy-4-(2',4',5'-trimethoxyphenyl)-(2E)-hexenoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 148826-19-1 Structure
  • Basic information

    1. Product Name: (+/-) methyl (4,5)-anti-5-hydroxy-4-(2',4',5'-trimethoxyphenyl)-(2E)-hexenoate
    2. Synonyms: (+/-) methyl (4,5)-anti-5-hydroxy-4-(2',4',5'-trimethoxyphenyl)-(2E)-hexenoate
    3. CAS NO:148826-19-1
    4. Molecular Formula:
    5. Molecular Weight: 310.347
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 148826-19-1.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 (4,5)-anti-5-hydroxy-4-(2',4',5'-trimethoxyphenyl)-(2E)-hexenoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-) methyl (4,5)-anti-5-hydroxy-4-(2',4',5'-trimethoxyphenyl)-(2E)-hexenoate(148826-19-1)
    11. EPA Substance Registry System: (+/-) methyl (4,5)-anti-5-hydroxy-4-(2',4',5'-trimethoxyphenyl)-(2E)-hexenoate(148826-19-1)
  • 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: 148826-19-1(Hazardous Substances Data)

148826-19-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148826-19-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,8,2 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 148826-19:
(8*1)+(7*4)+(6*8)+(5*8)+(4*2)+(3*6)+(2*1)+(1*9)=161
161 % 10 = 1
So 148826-19-1 is a valid CAS Registry Number.

148826-19-1Downstream Products

148826-19-1Relevant articles and documents

A facile chemoenzymatic route to optically active 4,5-disubstituted-2E-hexenoate derivatives. I

Akita,Umezawa,Takano,Ohyama,Matsukura,Oishi

, p. 55 - 63 (2007/10/02)

The reaction of (±) methyl 4,5-trans-epoxy-2E-hexenoate (2) with aromatic nucleophiles having an electron-donating group in the presence of BF3 · Et2O gave the 4,5-anti-5-hydroxy-4- or/and 2,5-anti-5-hydroxy-2-substituted products. T

A facile chemoenzymatic route to enantiomerically pure 4,5-disubstituted-2-hexenoae derivatives

Akita,Umezawa,Takano,Matsukura,Oishi

, p. 3094 - 3096 (2007/10/02)

The reaction of 4,5-epoxy-2-hexenoate 2 and various nucleophiles in the presence of BF3.Et2O predominantly gave the (4,5)-5-hydroxy-4-substituted compounds. Among them, (±)-(4,5)-anti-5-hydroxy-4-thiophenoxy ester 17 was enantioselec

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