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Methyl (3R,4S)-3--4,5-(isopropylidenedioxy)-pentanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 121614-06-0 Structure
  • Basic information

    1. Product Name: Methyl (3R,4S)-3--4,5-(isopropylidenedioxy)-pentanoate
    2. Synonyms:
    3. CAS NO:121614-06-0
    4. Molecular Formula:
    5. Molecular Weight: 423.625
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121614-06-0.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 (3R,4S)-3--4,5-(isopropylidenedioxy)-pentanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl (3R,4S)-3--4,5-(isopropylidenedioxy)-pentanoate(121614-06-0)
    11. EPA Substance Registry System: Methyl (3R,4S)-3--4,5-(isopropylidenedioxy)-pentanoate(121614-06-0)
  • 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: 121614-06-0(Hazardous Substances Data)

121614-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121614-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,6,1 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 121614-06:
(8*1)+(7*2)+(6*1)+(5*6)+(4*1)+(3*4)+(2*0)+(1*6)=80
80 % 10 = 0
So 121614-06-0 is a valid CAS Registry Number.

121614-06-0Relevant articles and documents

Ketene Silyl Acetal Chemistry; Diastereofacial Selectivity of 1,3-Addition of Chiral Nitrones

Kita, Yasuyuki,Tamura, Osamu,Itoh, Fumio,Kishino, Hiroko,Miki, Takashi,et al.

, p. 761 - 763 (1988)

The reaction of dimethyl-t-butylsiloxy-1-methoxyethene (1a) with the N-benzylnitrone (3a) produced the syn-1,3-adduct (4a) predominantly, while the reaction of dimethyl-t-butylsiloxy-1-t-butoxyethene (1b) with the N-diphenylmethylnitrone (3d) gave the ant

Chemistry of O-Silylated Ketene Acetals: Stereocontrolled Synthesis of 3-Benzoylamino-2,3-dideoxypentoses by a 1,3-Addition to Chiral Nitrones

Kita, Yasuyuki,Tamura, Osamu,Itoh, Fumio,Kishino, Hiroko,Miki, Takashi,et al.

, p. 2002 - 2007 (2007/10/02)

The stereochemistry of 1,3-addition of ketene acetals (1a,b) to the chiral nitrones (4a-d) derived from 2,3-O-isopropylidene-D-glyceraldehyde was examined.The reaction of ketene methyl tert-butyldimethylsilyl acetal (1a) with the N-benzylnitrone (4a) prod

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