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(1R,3R)-4,4,4-trichloro-1-phenylbutane-1,3-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1383976-99-5 Structure
  • Basic information

    1. Product Name: (1R,3R)-4,4,4-trichloro-1-phenylbutane-1,3-diol
    2. Synonyms: (1R,3R)-4,4,4-trichloro-1-phenylbutane-1,3-diol
    3. CAS NO:1383976-99-5
    4. Molecular Formula:
    5. Molecular Weight: 269.555
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1383976-99-5.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: (1R,3R)-4,4,4-trichloro-1-phenylbutane-1,3-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,3R)-4,4,4-trichloro-1-phenylbutane-1,3-diol(1383976-99-5)
    11. EPA Substance Registry System: (1R,3R)-4,4,4-trichloro-1-phenylbutane-1,3-diol(1383976-99-5)
  • 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: 1383976-99-5(Hazardous Substances Data)

1383976-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1383976-99-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,9,7 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1383976-99:
(9*1)+(8*3)+(7*8)+(6*3)+(5*9)+(4*7)+(3*6)+(2*9)+(1*9)=225
225 % 10 = 5
So 1383976-99-5 is a valid CAS Registry Number.

1383976-99-5Relevant articles and documents

Stereoselective synthesis of cis- or trans-2,4-disubstituted butyrolactones from Wynberg lactone

Ganta, Ashok,Shamshina, Julia L.,Cafiero, Lauren R.,Snowden, Timothy S.

, p. 5396 - 5405 (2012/09/08)

(R)-Wynberg lactone was used to prepare various asymmetric 2,4-disubstituted butyrolactones in three to four steps. Attainment of any possible stereoisomer, based upon commencement from (R)- or (S)-4- trichloromethyl-2-oxetanone, and the capacity to insta

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