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1,1'-(p-phenylenedicarbonyl)bis[hexahydro-2H-azepin-2-one], commonly known as HATU, is a chemical compound that serves as a coupling reagent in peptide synthesis. It is renowned for its high efficiency in facilitating the formation of peptide bonds between amino acids, particularly in solid-phase peptide synthesis. HATU is a white to off-white powder that is soluble in various organic solvents, making it a versatile component in the synthesis process.

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  • 2669-15-0 Structure
  • Basic information

    1. Product Name: 1,1'-(p-phenylenedicarbonyl)bis[hexahydro-2H-azepin-2-one]
    2. Synonyms: 1,1'-(p-phenylenedicarbonyl)bis[hexahydro-2H-azepin-2-one];1,1'-(1,4-Phenylenebiscarbonyl)bis(azacycloheptane-2-one);1,1'-(1,4-Phenylenedicarbonyl)bis(1,3,4,5,6,7-hexahydro-2H-azepin-2-one);1,1'-(1,4-Phenylenedicarbonyl)bis(hexahydro-1H-azepin-2-one)
    3. CAS NO:2669-15-0
    4. Molecular Formula: C20H24N2O4
    5. Molecular Weight: 356.41556
    6. EINECS: 220-209-2
    7. Product Categories: N/A
    8. Mol File: 2669-15-0.mol
  • Chemical Properties

    1. Melting Point: 191-193 °C(Solv: ethanol (64-17-5))
    2. Boiling Point: 591.2±46.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.237±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -2.41±0.20(Predicted)
    10. CAS DataBase Reference: 1,1'-(p-phenylenedicarbonyl)bis[hexahydro-2H-azepin-2-one](CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,1'-(p-phenylenedicarbonyl)bis[hexahydro-2H-azepin-2-one](2669-15-0)
    12. EPA Substance Registry System: 1,1'-(p-phenylenedicarbonyl)bis[hexahydro-2H-azepin-2-one](2669-15-0)
  • 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: 2669-15-0(Hazardous Substances Data)

2669-15-0 Usage

Uses

Used in Pharmaceutical Industry:
1,1'-(p-phenylenedicarbonyl)bis[hexahydro-2H-azepin-2-one] is used as a coupling reagent for the synthesis of peptide-based drugs. Its high efficiency in peptide bond formation contributes to the development of novel therapeutic agents, enhancing the production process and the quality of the final product.
Used in Biotechnology Industry:
In the biotechnology sector, 1,1'-(p-phenylenedicarbonyl)bis[hexahydro-2H-azepin-2-one] is utilized as a key component in the synthesis of research peptides. Its role in facilitating peptide bond formation aids in the creation of peptides for scientific studies and potential applications in various fields.
Safety Precautions:
It is crucial to handle 1,1'-(p-phenylenedicarbonyl)bis[hexahydro-2H-azepin-2-one] with care, as it can be harmful if ingested or inhaled. Additionally, it may cause irritation to the skin and eyes, necessitating proper protective measures during its use in laboratories and industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 2669-15-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,6 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2669-15:
(6*2)+(5*6)+(4*6)+(3*9)+(2*1)+(1*5)=100
100 % 10 = 0
So 2669-15-0 is a valid CAS Registry Number.

2669-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-(2-oxoazepane-1-carbonyl)benzoyl]azepan-2-one

1.2 Other means of identification

Product number -
Other names dodecahydro-1,1'-terephthaloyl-bis-azepin-2-one

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2669-15-0 SDS

2669-15-0Relevant articles and documents

Process for the preparation of amidoperoxycarboxylic acids

-

, (2008/06/13)

Process for the preparation of amidoperoxycarboxylic acids, comprising the process steps: ring opening of the N-acyllactam to give the corresponding amidocarboxylic acid and, subsequently, oxidation of the resulting amidocarboxylic acid to the correspondi

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