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267895-50-1

(4S,5R,6R,7S)-4,7-dibenzyloxymethyl-5,6-dihydroxy-5,6-O-methylethylidene-2-(N-benzyl)-imino-1,3-diazepane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 267895-50-1 Structure

  • Basic information

    1. Product Name: (4S,5R,6R,7S)-4,7-dibenzyloxymethyl-5,6-dihydroxy-5,6-O-methylethylidene-2-(N-benzyl)-imino-1,3-diazepane
    2. Synonyms:
    3. CAS NO:267895-50-1
    4. Molecular Formula:
    5. Molecular Weight: 515.652
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 267895-50-1.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: (4S,5R,6R,7S)-4,7-dibenzyloxymethyl-5,6-dihydroxy-5,6-O-methylethylidene-2-(N-benzyl)-imino-1,3-diazepane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S,5R,6R,7S)-4,7-dibenzyloxymethyl-5,6-dihydroxy-5,6-O-methylethylidene-2-(N-benzyl)-imino-1,3-diazepane(267895-50-1)
    11. EPA Substance Registry System: (4S,5R,6R,7S)-4,7-dibenzyloxymethyl-5,6-dihydroxy-5,6-O-methylethylidene-2-(N-benzyl)-imino-1,3-diazepane(267895-50-1)

  • 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: 267895-50-1(Hazardous Substances Data)

267895-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 267895-50-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,7,8,9 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 267895-50:
(8*2)+(7*6)+(6*7)+(5*8)+(4*9)+(3*5)+(2*5)+(1*0)=201
201 % 10 = 1
So 267895-50-1 is a valid CAS Registry Number.

267895-50-1Downstream Products

267895-50-1Relevant articles and documents

Synthesis of C2-symmetric guanidino-sugars as potent inhibitors of glycosidases

Le Merrer, Yves,Gauzy, Laurence,Gravier-Pelletier, Christine,Depezay, Jean-Claude

, p. 307 - 320 (2007/10/03)

A series of enantiomerically pure C2-Symmetric guanidino-sugars was synthesized from D-mannitol. The first method described involves direct opening of a bis-epoxide by guanidine, whereas the second one deals with a mercury-catalyzed transformation of a cyclic thiourea into a N,N',N'- trisubstituted guanidine as a key step. The biological activity of these compounds towards several glycosidases has been evaluated. One of them (5) was found to selectively inhibit α-L-fucosidase of bovin kidney (2.8 μM). (C) 2000 Elsevier Science Ltd.

Synthesis of C2-symmetrical cyclic guanidino-sugars from D-mannitol

Gauzy, Laurence,Le Merrer, Yves,Depezay, Jean-Claude

, p. 402 - 404 (2007/10/03)

An efficient method for the synthesis of C2-symmetrical cyclic guanidino-sugars has been developed from 1,2:5,6-dianhydro-3,4-O-methylethylidene-D-mannitol or L-iditol.

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