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154125-86-7

methyl 2-deoxy-3,4,6-tri-O-benzyl-2-(N-acetylamino)-α-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 154125-86-7 Structure

  • Basic information

    1. Product Name: methyl 2-deoxy-3,4,6-tri-O-benzyl-2-(N-acetylamino)-α-D-glucopyranoside
    2. Synonyms: methyl 2-deoxy-3,4,6-tri-O-benzyl-2-(N-acetylamino)-α-D-glucopyranoside
    3. CAS NO:154125-86-7
    4. Molecular Formula:
    5. Molecular Weight: 505.611
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 154125-86-7.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: methyl 2-deoxy-3,4,6-tri-O-benzyl-2-(N-acetylamino)-α-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-deoxy-3,4,6-tri-O-benzyl-2-(N-acetylamino)-α-D-glucopyranoside(154125-86-7)
    11. EPA Substance Registry System: methyl 2-deoxy-3,4,6-tri-O-benzyl-2-(N-acetylamino)-α-D-glucopyranoside(154125-86-7)

  • 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: 154125-86-7(Hazardous Substances Data)

154125-86-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154125-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,1,2 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 154125-86:
(8*1)+(7*5)+(6*4)+(5*1)+(4*2)+(3*5)+(2*8)+(1*6)=117
117 % 10 = 7
So 154125-86-7 is a valid CAS Registry Number.

154125-86-7Relevant articles and documents

Efficient syntheses of methyl 2-amino-2-deoxy-3,4,6-tri-o-benzyl-α-D-glucopyranoside and its 2-tert-butoxycarbonylamino- and 2-methylamino derivatives from N-acetyl-D-glucosamine

Henry, Christophe,Joly, Jean-Pierre,Chapleur, Yves

, p. 689 - 695 (1999)

The synthesis of the title compounds started with N-acetylglucosamine which was converted into the corresponding methyl glycoside and O-protected with benzyl groups. Subsequent N-protection as its N-BOC-N-acetyl derivative and sequential removal of the N-

Synthesis and characterization of monosaccharide derivatives and application of sugar-based prolinamides in asymmetric synthesis

Agarwal, Jyoti,Peddinti, Rama Krishna

, p. 6390 - 6406,17 (2020/09/16)

For the first time, the β-anomer of N-acetylglucosamine derivative methyl 2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranoside (9b) was synthesized, isolated, and used in the synthesis of sugar-based primary amine 4b. Sugar-based primary amine 5a, a

Glucosamine-based primary amines as organocatalysts for the asymmetric aldol reaction

Agarwal, Jyoti,Peddinti, Rama Krishna

, p. 3502 - 3505 (2011/06/21)

Glucosamine derivatives have been synthesized starting from commercially available N-acetyl-D-glucosamine/glucosamine hydrochloride and have been employed successfully as efficient organocatalysts for the direct asymmetric aldol reaction between cyclohexa

Synthesis of Tc-99m labeled glucosamino-Asp-cyclic(Arg-Gly-Asp-d-Phe-Lys) as a potential angiogenesis imaging agent

Lee, Byung Chul,Sung, Hyun Ju,Kim, Ji Sun,Jung, Kyung-Ho,Choe, Yearn Seong,Lee, Kyung-Han,Chi, Dae Yoon

, p. 7755 - 7764 (2008/03/28)

Angiogenesis imaging agents for single photon emission computed tomography (SPECT) play a role in diagnosing tumor-induced angiogenesis as well as tumor metastasis. We synthesized and evaluated radiolabeled RGD glycopeptides by incorporation of the [

26. A 1H-NMR spectroscopic investigation of the conformation of the acetamido group in some derivatives of N-acetyl-D-allosamine and -D-glucosamine

Fowler, Paul,Bernet, Bruno,Vasella, Andrea

, p. 269 - 287 (2007/10/03)

The population of the conformations obtained by rotation around the C(2)-N and the N-C(O) bonds of AllNAc, GlcNAc, and GlcNMeAc derivatives was investigated by 1H-NMR spectroscopy. The AllNAc-derived α -D- and β -D-pyranosides 4-7, the AllNAc d

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