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52612-38-1

(S,E)-3-(2,6,6-trimethylcyclohex-2-en-1-yl)acrylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52612-38-1 Structure

  • Basic information

    1. Product Name: (S,E)-3-(2,6,6-trimethylcyclohex-2-en-1-yl)acrylic acid
    2. Synonyms: (S,E)-3-(2,6,6-trimethylcyclohex-2-en-1-yl)acrylic acid
    3. CAS NO:52612-38-1
    4. Molecular Formula:
    5. Molecular Weight: 194.274
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52612-38-1.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: (S,E)-3-(2,6,6-trimethylcyclohex-2-en-1-yl)acrylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S,E)-3-(2,6,6-trimethylcyclohex-2-en-1-yl)acrylic acid(52612-38-1)
    11. EPA Substance Registry System: (S,E)-3-(2,6,6-trimethylcyclohex-2-en-1-yl)acrylic acid(52612-38-1)

  • 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: 52612-38-1(Hazardous Substances Data)

52612-38-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52612-38-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,1 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52612-38:
(7*5)+(6*2)+(5*6)+(4*1)+(3*2)+(2*3)+(1*8)=101
101 % 10 = 1
So 52612-38-1 is a valid CAS Registry Number.

52612-38-1Downstream Products

52612-38-1Relevant articles and documents

Total Synthesis and Stereochemical Confirmation of Heliolactone

Woo, Stone,McErlean, Christopher S. P.

, p. 4215 - 4218 (2019/06/04)

Until now, the relative stereochemistry of the noncanonical strigolactone, heliolactone, has remained ambiguous. The total synthesis of heliolactone is described, with the key bond-forming event being a Stille cross-coupling that relied upon a reversal of

Synthesis and anti-metastatic effects of novel chiral ionone alkaloid derivatives

Fang, Hai-Jun,Shou, Xiao-Ai,Liu, Qian,Gan, Chun-Chun,Duan, Hong-Quan,Qin, Nan

, p. 245 - 253 (2015/07/08)

Abstract Novel chiral ionone alkaloid derivatives were synthesized and evaluated their anti-metastatic effects in human MDA-MB-231 breast cancer cells. The chiral center C-6 of derivatives exerted an important role in response to the anti-metastatic activ

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