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Acetic acid (1S,2R,3R,4S,6R)-2-acetoxy-4,6-diazido-3-chloromethoxy-cyclohexyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 609342-43-0 Structure
  • Basic information

    1. Product Name: Acetic acid (1S,2R,3R,4S,6R)-2-acetoxy-4,6-diazido-3-chloromethoxy-cyclohexyl ester
    2. Synonyms: Acetic acid (1S,2R,3R,4S,6R)-2-acetoxy-4,6-diazido-3-chloromethoxy-cyclohexyl ester
    3. CAS NO:609342-43-0
    4. Molecular Formula:
    5. Molecular Weight: 346.73
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 609342-43-0.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: Acetic acid (1S,2R,3R,4S,6R)-2-acetoxy-4,6-diazido-3-chloromethoxy-cyclohexyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetic acid (1S,2R,3R,4S,6R)-2-acetoxy-4,6-diazido-3-chloromethoxy-cyclohexyl ester(609342-43-0)
    11. EPA Substance Registry System: Acetic acid (1S,2R,3R,4S,6R)-2-acetoxy-4,6-diazido-3-chloromethoxy-cyclohexyl ester(609342-43-0)
  • 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: 609342-43-0(Hazardous Substances Data)

609342-43-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 609342-43-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,9,3,4 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 609342-43:
(8*6)+(7*0)+(6*9)+(5*3)+(4*4)+(3*2)+(2*4)+(1*3)=150
150 % 10 = 0
So 609342-43-0 is a valid CAS Registry Number.

609342-43-0Downstream Products

609342-43-0Relevant articles and documents

The synthesis and 16S A-site rRNA recognition of carbohydrate-free aminoglycosides

Wang, Xiaojing,Migawa, Michael T.,Sannes-Lowery, Kristin A.,Swayze, Eric E.

, p. 4919 - 4922 (2007/10/03)

The first carbohydrate-free aminoglycoside analogs bearing the 2-deoxystreptamine moiety were synthesized from asymmetrically protected 2-deoxystrepamine and subsequently demonstrated to have significant binding to the 16S A-site rRNA target and moderate

Antimicrobial 2-deoxystreptamine compounds

-

Page column 22, (2010/02/07)

The present invention is directed to analogs of aminoglycoside compounds of the class having a glycosylated 2-deoxystreptamine (2-DOS) ring as well as their preparation and use as prophylactic or therapeutics against microbial infection. Compounds of the

Design and synthesis of paromomycin-related heterocycle-substituted aminoglycoside mimetics based on a mass spectrometry RNA-binding assay

Ding, Yili,Hofstadler, Steven A.,Swayze, Eric E.,Risen, Lisa,Griffey, Richard H.

, p. 3409 - 3412 (2007/10/03)

A good starting point for the design of potent bactericidal compounds is the aminoglycoside paromomycin (1). The A-ring (shown in red) was replaced with a range of heterocycles. An ESIMS-based RNA-binding assay was used to screen the binding affinities of

An efficient synthesis of mimetics of neamine for RNA recognition.

Ding,Hofstadler,Swayze,Griffey

, p. 1621 - 1623 (2007/10/03)

As mimetics of neamine, several 4-heterocyclic 2-deoxystreptamine derivatives were chemically synthesized for RNA recognition. Conversion of 4-methylthiomethyl-5,6-di-O-acetyl-diazido-2-deoxystreptamine to the 4-chloromethyl derivative followed by reactions with different nuclophilic reagents gave the 4-heterocyclic 2-deoxystreptamine derivatives in satisfactory yields.

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