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125827-01-2

3A-amino-3A-deoxy-β-cyclodextrin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125827-01-2 Structure

  • Basic information

    1. Product Name: 3A-amino-3A-deoxy-β-cyclodextrin
    2. Synonyms: 3A-amino-3A-deoxy-β-cyclodextrin
    3. CAS NO:125827-01-2
    4. Molecular Formula:
    5. Molecular Weight: 1134.01
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125827-01-2.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: 3A-amino-3A-deoxy-β-cyclodextrin(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3A-amino-3A-deoxy-β-cyclodextrin(125827-01-2)
    11. EPA Substance Registry System: 3A-amino-3A-deoxy-β-cyclodextrin(125827-01-2)

  • 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: 125827-01-2(Hazardous Substances Data)

125827-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125827-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,8,2 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 125827-01:
(8*1)+(7*2)+(6*5)+(5*8)+(4*2)+(3*7)+(2*0)+(1*1)=122
122 % 10 = 2
So 125827-01-2 is a valid CAS Registry Number.

125827-01-2Downstream Products

125827-01-2Relevant articles and documents

Cyclodextrin retinylidene: A biomimetic kinetic trap model for rhodopsin

Kpegba, Kafui,Murtha, Matthew,Nesnas, Nasri

, p. 1523 - 1526 (2006)

All trans retinal was attached to both the primary face and the secondary face of β-cyclodextrin via a Schiff base linkage, analogous to that in rhodopsin. The new models were evaluated and compared with n-butylamine retinylidene Schiff base for their rates of hydrolysis, and factors that influence such rates. Competition studies using adamantane carboxylate demonstrated the kinetic trap theory by diminishing the binding of retinal in the cyclodextrin, thereby augmenting the rate of hydrolysis. NMR experiments indicate that the retinylidene is most probably bound in the form of a dimer.

Functionalization of Cyclodextrins via Reactions of 2,3-Anhydrocyclodextrins

Yuan, De-Qi,Tahara, Tsutomu,Chen, Wen-Hua,Okabe, Yuji,Yang, Cheng,Yagi, Youichi,Nogami, Yasuyoshi,Fukudome, Makoto,Fujita, Kahee

, p. 9456 - 9466 (2007/10/03)

Three types of reactions of 2,3-anhydro-β-cyclodextrins, namely nucleophilic ring-opening, reduction to 2-enopyranose, and reduction to 3-deoxypyranose, have been investigated to regio- and stereoselectively functionalize the secondary face of β-cyclodext

Synthesis and Chiral Recognition Property of 3-Acetylamino-3-deoxy-β-cyclodextrin

Murakami, Teiichi,Harata, Kazuaki,Morimoto, Satoshi

, p. 553 - 556 (2007/10/02)

Mono(3-acetylamino-3-deoxy)-β-cyclodextrin (4) was firstly prepared via regioselective ring opening of manno-epoxide by ammonia. 1H-NMR investigation clearly demonstrated that 4 recognized the chirality of mandelic acids and N-acetyl-phenyl-glycine by the formation of diastereomeric inclusion complexes.

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