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207613-07-8

N-(carboxymethyl)-N-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)propyl]-mono(4-meth is a complex chemical compound that is a derivative of pyrrole, a five-membered heterocyclic compound containing a nitrogen atom. It contains carboxylic acid and various functional groups, including carboxymethyl and 4-methyl groups. The specific structure and properties of this compound would need to be further analyzed and evaluated to understand its potential uses and effects.

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  • 2-[carboxymethyl-[3-(2,5-dioxopyrrol-1-yl)propyl]amino]acetic acid,4-methylbenzenesulfonate

    Cas No: 207613-07-8

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  • N-(carboxymethyl)-N-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)propyl]-mono(4-meth

    Cas No: 207613-07-8

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  • Glycine,N-(carboxymethyl)-N-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)propyl]-

    Cas No: 207613-07-8

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  • 207613-07-8 Structure

  • Basic information

    1. Product Name: N-(carboxymethyl)-N-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)propyl]-mono(4-meth
    2. Synonyms: N-(carboxymethyl)-N-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)propyl]-mono(4-meth;N-(Carboxymethyl)-N-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)propyl]glycine mono(4-methylbenzenesulfonate)
    3. CAS NO:207613-07-8
    4. Molecular Formula: C11H14N2O6
    5. Molecular Weight: 442.44
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 207613-07-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(carboxymethyl)-N-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)propyl]-mono(4-meth(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(carboxymethyl)-N-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)propyl]-mono(4-meth(207613-07-8)
    11. EPA Substance Registry System: N-(carboxymethyl)-N-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)propyl]-mono(4-meth(207613-07-8)

  • 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: 207613-07-8(Hazardous Substances Data)

207613-07-8 Usage

Uses

N-(carboxymethyl)-N-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)propyl]-mono(4-meth can be used in various applications, including pharmaceuticals and organic synthesis, due to its unique structure and functional groups. However, further research and analysis would be required to determine its specific uses and effects in these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 207613-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,6,1 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 207613-07:
(8*2)+(7*0)+(6*7)+(5*6)+(4*1)+(3*3)+(2*0)+(1*7)=108
108 % 10 = 8
So 207613-07-8 is a valid CAS Registry Number.

207613-07-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[carboxymethyl-[3-(2,5-dioxopyrrol-1-yl)propyl]amino]acetic acid,4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:207613-07-8 SDS

207613-07-8Downstream Products

207613-07-8Relevant articles and documents

Facile synthesis of maleimide bifunctional linkers

King, H.Dalton,Dubowchik, Gene M,Walker, Michael A

, p. 1987 - 1990 (2007/10/03)

The synthesis of maleimide containing derivatives capable of serving as linkers for the conjugation of proteins is described. These compounds differ from previously reported linkers by having multiple sites available for drug attachment. Compounds 3a, 3b,

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