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CAS

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1360452-45-4

C12H18O4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1360452-45-4 Structure

  • Basic information

    1. Product Name: C12H18O4
    2. Synonyms: C12H18O4
    3. CAS NO:1360452-45-4
    4. Molecular Formula:
    5. Molecular Weight: 226.273
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1360452-45-4.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: C12H18O4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C12H18O4(1360452-45-4)
    11. EPA Substance Registry System: C12H18O4(1360452-45-4)

  • 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: 1360452-45-4(Hazardous Substances Data)

1360452-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1360452-45-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,4,5 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1360452-45:
(9*1)+(8*3)+(7*6)+(6*0)+(5*4)+(4*5)+(3*2)+(2*4)+(1*5)=134
134 % 10 = 4
So 1360452-45-4 is a valid CAS Registry Number.

1360452-45-4Upstream product

1360452-45-4Relevant articles and documents

Concise synthesis of (+)-conduritol F and inositol analogues from naturally available (+)-proto-quercitol and their glucosidase inhibitory activity

Worawalai, Wisuttaya,Rattanangkool, Eakkaphon,Vanitcha, Avassaya,Phuwapraisirisan, Preecha,Wacharasindhu, Sumrit

, p. 1538 - 1540 (2012)

An effective synthesis of (+)-conduritol F, (+)-chiro- and (+)-epi-inositols from naturally available (+)- proto-quercitol is described. This synthetic method provides a concise synthesis of cyclitols in enantiomerically pure form. Of the synthesized cyclitols, (+)-conduritol F potently inhibits type I α-glucosidase with an IC50 value of 86.1 lM, which is five times greater than the standard antidiabetic drug, acarbose.

Potent chemical chaperone compounds for GM1-gangliosidosis: N-substituted (+)-conduramine F-4 derivatives

Kuno, Shinichi,Higaki, Katsumi,Takahashi, Atsushi,Nanba, Eiji,Ogawa, Seiichiro

, p. 306 - 310 (2015/03/18)

The development of second-generation valienamine-type chemical chaperones for GM1-gangliosidosis is described. Several N-substituted (+)-conduramine F-4 derivatives were designed as novel chemical chaperones based on a lead chaperone compound, N-octyl-4-epi-β-valienamine, to decrease the inhibitory activity while increasing the enzyme enhancement activity. Among the derivatives synthesized during this study, a conduramine derivative with an N-cyclohexylmethyl group has demonstrated significant enhancement of R201C mutated β-galactosidase activity. This journal is

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