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133024-90-5

N-Cbz-N,N-bis2-[(methylsulfonyl)oxy]ethyl-amine is a chemical compound that is commonly used in pharmaceutical and organic synthesis. It is a derivative of amines and has a Cbz protecting group, which is often used in peptide synthesis. The presence of two bis2-[(methylsulfonyl)oxy]ethyl groups makes it a potentially useful building block for chemical reactions. The methylsulfonyl groups can also act as protecting groups, allowing for selective manipulation of the amine functionality. Overall, this compound has potential applications in the field of medicinal chemistry and drug development, as well as in the synthesis of organic compounds.

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  • 133024-90-5 Structure

  • Basic information

    1. Product Name: N-Cbz-N,N-bis{2-[(methylsulfonyl)oxy]ethyl}-amine
    2. Synonyms: N-Cbz-N,N-bis{2-[(methylsulfonyl)oxy]ethyl}-amine
    3. CAS NO:133024-90-5
    4. Molecular Formula: C14H21NO8S2
    5. Molecular Weight: 395.45
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133024-90-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 619.0±55.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.378±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -1.88±0.70(Predicted)
    10. CAS DataBase Reference: N-Cbz-N,N-bis{2-[(methylsulfonyl)oxy]ethyl}-amine(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-Cbz-N,N-bis{2-[(methylsulfonyl)oxy]ethyl}-amine(133024-90-5)
    12. EPA Substance Registry System: N-Cbz-N,N-bis{2-[(methylsulfonyl)oxy]ethyl}-amine(133024-90-5)

  • 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: 133024-90-5(Hazardous Substances Data)

133024-90-5 Usage

Uses

Used in Pharmaceutical and Organic Synthesis:
N-Cbz-N,N-bis2-[(methylsulfonyl)oxy]ethyl-amine is used as a building block for chemical reactions in the pharmaceutical and organic synthesis industries. Its Cbz protecting group and bis2-[(methylsulfonyl)oxy]ethyl groups make it a versatile compound for the synthesis of various organic compounds and the development of new drugs.
Used in Peptide Synthesis:
In the field of peptide synthesis, N-Cbz-N,N-bis2-[(methylsulfonyl)oxy]ethyl-amine is used as a protecting group for amines. The methylsulfonyl groups allow for selective manipulation of the amine functionality, enabling the synthesis of complex peptide structures with greater control and precision.
Used in Medicinal Chemistry:
N-Cbz-N,N-bis2-[(methylsulfonyl)oxy]ethyl-amine is used in medicinal chemistry for the development of new drugs. Its unique structure and functional groups make it a promising candidate for the design and synthesis of novel therapeutic agents with potential applications in various medical fields.

Check Digit Verification of cas no

The CAS Registry Mumber 133024-90-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,2 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 133024-90:
(8*1)+(7*3)+(6*3)+(5*0)+(4*2)+(3*4)+(2*9)+(1*0)=85
85 % 10 = 5
So 133024-90-5 is a valid CAS Registry Number.

133024-90-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-methylsulfonyloxyethyl(phenylmethoxycarbonyl)amino]ethyl methanesulfonate

1.2 Other means of identification

Product number -
Other names N-benzyloxycarbonyldiethanolamine dimesylate

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:133024-90-5 SDS

133024-90-5Relevant articles and documents

Synthesis and metal-ion binding properties of monoazathiacrown ethers

Tanaka,Nakamura,Ikeda,Ikeda,Ando,Shibutani,Yajima,Kimura

, p. 7008 - 7012 (2007/10/03)

Synthetic procedures for monoazathiacrown ethers were explored, and monoazatrithia-12-crown-4, monoazatetrathia-15-crown-5, and monoazapentathia-18-crown-6 were obtained in moderate yields by the reaction of bis(2-chloroethyl)amine with the appropriate dithiols in the presence of lithium hydroxide in THF. To evaluate metal-ion binding properties of the monoazathiacrown ethers by solvent extraction, lipophilic dodecyl and dodecanoyl groups were incorporated onto the monoazathiacrown ethers. The solvent extraction experiments suggested that monoazathiacrown ethers have Ag+ and Hg2+ selectivities and that the relative selectivity between Ag+ and Hg2+ depends on their nitrogen atom properties and numbers of sulfur atoms reflecting the respective affinities of nitrogen and sulfur atoms to Hg2+ and Ag+. An interesting ability to bind Mg2+ was observed in the case of N-dodecyl monoazatrithia-12-crown-4.

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