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  • 51764-86-4 Structure
  • Basic information

    1. Product Name: 2-hydroxycinnamyl alcohol
    2. Synonyms: 2-hydroxycinnamyl alcohol
    3. CAS NO:51764-86-4
    4. Molecular Formula:
    5. Molecular Weight: 150.177
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 51764-86-4.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: 2-hydroxycinnamyl alcohol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-hydroxycinnamyl alcohol(51764-86-4)
    11. EPA Substance Registry System: 2-hydroxycinnamyl alcohol(51764-86-4)
  • 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: 51764-86-4(Hazardous Substances Data)

51764-86-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51764-86-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,7,6 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51764-86:
(7*5)+(6*1)+(5*7)+(4*6)+(3*4)+(2*8)+(1*6)=134
134 % 10 = 4
So 51764-86-4 is a valid CAS Registry Number.

51764-86-4Relevant articles and documents

Inhibition of chitin synthases and antifungal activities by 2′-benzoyloxycinnamaldehyde from Pleuropterus ciliinervis and its derivatives

Kang, Tae Hoon,Hwang, Eui Il,Yun, Bong Sik,Park, Ki Duk,Kwon, Byoung Mog,Shin, Chul Soo,Kim, Sung Uk

, p. 598 - 602 (2008/02/02)

In the course of search for potent chitin synthase inhibitors from natural resources, a novel chitin synthases inhibitor, 2′-benzoyloxycinnamaldehyde (2′-BCA) (I), was isolated from the aerial parts of Pleuropterus ciliinervis NAKAI. 2′-BCA inhibited chit

The constituents and synthesis of cryptamygin-A from the stem bark of Cryptocarya amygadalina

Chan, Yu-Yi,Wu, Chia-Hung,Wu, Shwu-Jen,Wu, Tian-Shung

, p. 263 - 268 (2007/10/03)

Three new benzenoid compounds, namely cryptamygin-A, -B and -C together with eleven known compounds were isolated from the stem bark of Cryptocarya amygadalina. Their structures were elucidated by spectral analysis. The synthesis of cryptamygin-A is also

Cinnamaldehydes inhibit cyclin dependent kinase 4/cyclin D1

Jeong, Ha-Won,Kim, Mi-Ran,Son, Kwang-Hee,Young Han, Mi,Ha, Ji-Hong,Garnier, Matthieu,Meijer, Laurent,Kwon, Byoung-Mog

, p. 1819 - 1822 (2007/10/03)

A series of cinnamaldehydes was synthesized for the study of inhibitory activity against cyclin dependent kinases (CDKs). A couple of compounds selectively inhibited cyclin D1-CDK4 with an IC50 value of 7-18 μM. (C) 2000 Elsevier Science Ltd. All rights reserved.

Synthesis and biological activity of cinnamaldehydes as angiogenesis inhibitors

Kwon, Byoung-Mog,Lee, Seung-Ho,Cho, Young-Kwon,Bok, Song-Hae,So, Seung-Ho,Youn, Mi-Ran,Chang, Soo-Ik

, p. 2473 - 2476 (2007/10/03)

A series of 2-hydroxycinnamaldehyde derivatives was synthesized for examing a structure-activity relationship for inhibition of angiogenesis. The anti-angiogenic effects of 2'-substituted cinnamaldehydes and related analogs were determined in a chick embryo chorioallantoic membrane assay system.

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