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C22H33N5O6 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Prop-2-enyl N-[(2S)-1-[[(2S)-5-(carbamoylamino)-1-[4-(hydroxymethyl)anilino]-1-oxopentan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]carbamate;1608127-09-8

    Cas No: 1608127-09-8

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  • prop-2-en-1-yl N-[(1S)-1-{[(1S)-4-(carbamoylamino)-1-{[4-(hydroxymethyl)phenyl]carbamoyl}butyl]carbamoyl}-2-methylpropyl]carbamate

    Cas No: 1608127-09-8

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  • 1608127-09-8 Structure
  • Basic information

    1. Product Name: C22H33N5O6
    2. Synonyms: C22H33N5O6
    3. CAS NO:1608127-09-8
    4. Molecular Formula:
    5. Molecular Weight: 463.534
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1608127-09-8.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: C22H33N5O6(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H33N5O6(1608127-09-8)
    11. EPA Substance Registry System: C22H33N5O6(1608127-09-8)
  • 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: 1608127-09-8(Hazardous Substances Data)

1608127-09-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1608127-09-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,8,1,2 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1608127-09:
(9*1)+(8*6)+(7*0)+(6*8)+(5*1)+(4*2)+(3*7)+(2*0)+(1*9)=148
148 % 10 = 8
So 1608127-09-8 is a valid CAS Registry Number.

1608127-09-8Relevant articles and documents

MODIFIED ANTIBODY, ANTIBODY-CONJUGATE AND PROCESS FOR THE PREPARATION THEREOF

-

, (2014/05/24)

The present invention relates to an antibody comprising a GlcNAc-S(A)x substituent, wherein S(A)x is a sugar derivative comprising x functional groups A wherein A is independently selected from the group consisting of an azido group, a keto group and an alkynyl group and x is 1, 2, 3 or 4, wherein said GlcNAc-S(A)x substituent is bonded to the antibody via CI of the N-acetylglucosamine of said GlcNAc-S(A)x substituent, and wherein said N-acetylglucosamine is optionally fucosylated. The invention also relates to an antibody-conjugate, in particular to an antibody- conjugate according to the Formula (20) or (20b), wherein AB is an antibody, S is a sugar or a sugar derivative, D is a molecule of interest, and wherein said N- acetylglucosamine is optionally fucosylated (b is 0 or 1). The invention further relates to a process for the preparation of a modified antibody, to a process for the preparation of an antibody-conjugate, and to said antibody-conjugate for use as a medicament. In addition, the invention relates to a kit of parts comprising an azide-modified antibody and a linker-conjugate, wherein said linker-conjugate comprises a (hetero)cycloalkynyl group and one or more molecules of interest.

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