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(S)-4-BOC-6,6-DIMETHYL-MORPHOLINE-3-CARBOXYLIC ACID, also known as BOC-protected (S)-6,6-dimethylmorpholine-3-carboxylic acid, is a chemical compound that serves as a crucial intermediate in the synthesis of pharmaceuticals and biologically active compounds. (S)-4-BOC-6,6-DIMETHYL-MORPHOLINE-3-CARBOXYLIC ACID features a BOC (tert-butoxycarbonyl) protecting group, which is strategically added to the amine functional group to prevent side reactions during the synthesis process. Its role in peptide synthesis and the production of small organic molecules makes it a vital component in the pharmaceutical and biotechnology industries, contributing to the development and production of innovative drugs and therapeutic compounds.

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  • (3S)-6,6-Dimethyl-morpholine-3,4-dicarboxylic acid 4-tert-butyl ester

    Cas No: 783349-78-0

  • USD $ 1.9-2.9 / Gram

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  • 783349-78-0 Structure
  • Basic information

    1. Product Name: (S)-4-BOC-6,6-DIMETHYL-MORPHOLINE-3-CARBOXYLIC ACID
    2. Synonyms: (S)-4-BOC-6,6-DIMETHYL-MORPHOLINE-3-CARBOXYLIC ACID;(S)-6,6-Dimethyl-morpholine-3,4-dicarboxylic acid 4-tert-butyl ester;(S)-4-(tert-Butoxycarbonyl)-6,6-diMethylMorpholine-3-carboxylic acid;(3S)-6,6-Dimethyl-morpholine-3,4-dicarboxylic acid 4-tert-butyl ester;(S)-4-Boc-6,6-Dimethyl-morpholine-3-carboxylic acid, >=98%
    3. CAS NO:783349-78-0
    4. Molecular Formula: C12H21 N O5
    5. Molecular Weight: 259.30
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 783349-78-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 373.973°C at 760 mmHg
    3. Flash Point: 179.973°C
    4. Appearance: white crystalline powder
    5. Density: 1.145g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 3.55±0.40(Predicted)
    10. CAS DataBase Reference: (S)-4-BOC-6,6-DIMETHYL-MORPHOLINE-3-CARBOXYLIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: (S)-4-BOC-6,6-DIMETHYL-MORPHOLINE-3-CARBOXYLIC ACID(783349-78-0)
    12. EPA Substance Registry System: (S)-4-BOC-6,6-DIMETHYL-MORPHOLINE-3-CARBOXYLIC ACID(783349-78-0)
  • 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: 783349-78-0(Hazardous Substances Data)

783349-78-0 Usage

Uses

Used in Pharmaceutical Industry:
(S)-4-BOC-6,6-DIMETHYL-MORPHOLINE-3-CARBOXYLIC ACID is used as a key intermediate for the synthesis of various pharmaceuticals, facilitating the creation of new drugs and therapeutic compounds. Its presence in the synthesis process ensures the protection of amine groups, allowing for cleaner reactions and the production of more specific and effective medications.
Used in Biotechnology Industry:
In the biotechnology sector, (S)-4-BOC-6,6-DIMETHYL-MORPHOLINE-3-CARBOXYLIC ACID is utilized as a component in the synthesis of biologically active compounds. Its protective role in peptide synthesis is essential for the development of bioactive molecules with potential applications in research, diagnostics, and therapeutics.
Used in Peptide Synthesis:
(S)-4-BOC-6,6-DIMETHYL-MORPHOLINE-3-CARBOXYLIC ACID is used as a protecting agent in peptide synthesis, ensuring that the amine functional groups remain intact and unreacted during the synthesis process. This protection allows for the controlled formation of peptide bonds and the production of peptides with specific sequences and functions.
Used in Small Organic Molecule Production:
(S)-4-BOC-6,6-DIMETHYL-MORPHOLINE-3-CARBOXYLIC ACID is also used as a building block in the production of small organic molecules, which are essential in various chemical and pharmaceutical applications. The BOC-protected (S)-6,6-dimethylmorpholine-3-carboxylic acid contributes to the synthesis of these molecules, enhancing their stability and reactivity in targeted reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 783349-78-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,3,3,4 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 783349-78:
(8*7)+(7*8)+(6*3)+(5*3)+(4*4)+(3*9)+(2*7)+(1*8)=210
210 % 10 = 0
So 783349-78-0 is a valid CAS Registry Number.

783349-78-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-4-(tert-Butoxycarbonyl)-6,6-dimethylmorpholine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names (3S)-6,6-dimethyl-4-[(2-methylpropan-2-yl)oxycarbonyl]morpholine-3-carboxylic acid

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:783349-78-0 SDS

783349-78-0Upstream product

783349-78-0Downstream Products

783349-78-0Relevant articles and documents

Beta-carbolines useful for treating inflammatory disease

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Page/Page column 101, (2010/02/14)

This invention provides beta-carboline compounds of formula III-A-aa: wherein Q, G, R1, R2, R3, and R6b are as described in the specification. The compounds are useful for treating diseases such as inflammatory diseases and cancer.

BETA-CARBOLINES USEFUL FOR TREATING INFLAMMATORY DISEASE

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Page 118, (2010/02/09)

This invention provides beta-carboline compounds of formula (I) wherein Ring A is a substituted pyridinyl, pyrimidinyl, morpholinyl, piperidinyl, piperazinyl, pyrrolidinyl, pyranyl, tetrahydrofuranyl, cyclohexyl, cyclopentyl or thiomorpholinyl ring and R1, R2 and R3 are as described in the specification. The compounds are IKK-2 inhibitors that are useful for treating IKK-2 mediated diseases such as inflammatory diseases and cancer.

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