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N-ME-PHE-OBZL P-TOSYLATE is a chemical compound derived from N-methyl-L-phenylalanine, featuring a p-tosylate group attached to it. This modification serves as a protecting group for the amino acid phenylalanine, crucial in organic synthesis for shielding the amino group during specific chemical reactions. This selective protection allows for the modification of other molecular parts without interference, making N-ME-PHE-OBZL P-TOSYLATE an essential component in the synthesis of intricate organic molecules and pharmaceuticals.

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  • 40298-25-7 Structure
  • Basic information

    1. Product Name: N-ME-PHE-OBZL P-TOSYLATE
    2. Synonyms: H-MEPHE-OBZL TOS-OH;N-ME-PHE-OBZL P-TOSYLATE;N-ME-PHE-OBZL TOSOH;N-ME-PHENYLALANINE-OBZL P-TOSYLATE;N-ALPHA-METHYL-L-PHENYLALANINE BENZYL ESTER 4-TOLUENESULFONATE SALT;N-ALPHA-METHYL-L-PHENYLANINE BENZYL ESTER P-TOSYLATE;N-Me-Phe-OBzl;N-Methyl-L-phenylalanine phenylmethyl ester 4-methylbenzenesulfonate
    3. CAS NO:40298-25-7
    4. Molecular Formula: C24H27NO5S
    5. Molecular Weight: 441.54
    6. EINECS: N/A
    7. Product Categories: amino acids
    8. Mol File: 40298-25-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /Solid
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: N-ME-PHE-OBZL P-TOSYLATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-ME-PHE-OBZL P-TOSYLATE(40298-25-7)
    11. EPA Substance Registry System: N-ME-PHE-OBZL P-TOSYLATE(40298-25-7)
  • 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: 40298-25-7(Hazardous Substances Data)

40298-25-7 Usage

Uses

Used in Organic Synthesis:
N-ME-PHE-OBZL P-TOSYLATE is used as a protecting group for the amino acid phenylalanine, ensuring that the amino group remains intact during chemical reactions. This selective protection is vital for the synthesis of complex organic molecules where the integrity of the amino group must be preserved.
Used in Pharmaceutical Compounds:
In the pharmaceutical industry, N-ME-PHE-OBZL P-TOSYLATE is utilized as a key intermediate in the development of various drug compounds. Its role in protecting the amino group of phenylalanine allows chemists to create sophisticated drug molecules with specific functionalities and therapeutic properties.
Used in Research and Development:
N-ME-PHE-OBZL P-TOSYLATE is also employed in research settings to explore new synthetic pathways and develop innovative methods for the synthesis of complex organic and pharmaceutical compounds. Its protective properties enable researchers to investigate the reactivity and selectivity of various chemical reactions involving phenylalanine derivatives.

Check Digit Verification of cas no

The CAS Registry Mumber 40298-25-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,9 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40298-25:
(7*4)+(6*0)+(5*2)+(4*9)+(3*8)+(2*2)+(1*5)=107
107 % 10 = 7
So 40298-25-7 is a valid CAS Registry Number.

40298-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl (2S)-2-(methylamino)-3-phenylpropanoate,4-methylbenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names N-Me-Phe-Obzl p-Tosylate

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:40298-25-7 SDS

40298-25-7Upstream product

40298-25-7Relevant articles and documents

Benzyl compounds which inhibit leukocyte adhesion mediated by VLA-4

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Page column 52-53, (2010/01/31)

Disclosed are compounds which bind VLA-4. Certain of these compounds also inhibit leukocyte adhesion and, in particular, leukocyte adhesion mediated by VLA-4. Such compounds are useful in the treatment of inflammatory diseases in a mammalian patient, e.g., human, wherein the disease may be, for example, asthma, Alzheimer's disease, atherosclerosis, AIDS dementia, diabetes, inflammatory bowel disease, rheumatoid arthritis, tissue transplantation, tumor metastasis and myocardial ischemia. The compounds can also be administered for the treatment of inflammatory brain diseases such as multiple sclerosis.

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