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25442-39-1

Benzoic acid, 4-[[[[(1,1-dimethylethoxy)carbonyl]amino]acetyl]amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 25442-39-1 Structure

  • Basic information

    1. Product Name: Benzoic acid, 4-[[[[(1,1-dimethylethoxy)carbonyl]amino]acetyl]amino]-
    2. Synonyms:
    3. CAS NO:25442-39-1
    4. Molecular Formula: C14H18N2O5
    5. Molecular Weight: 294.307
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 25442-39-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzoic acid, 4-[[[[(1,1-dimethylethoxy)carbonyl]amino]acetyl]amino]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 4-[[[[(1,1-dimethylethoxy)carbonyl]amino]acetyl]amino]-(25442-39-1)
    11. EPA Substance Registry System: Benzoic acid, 4-[[[[(1,1-dimethylethoxy)carbonyl]amino]acetyl]amino]-(25442-39-1)

  • 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: 25442-39-1(Hazardous Substances Data)

25442-39-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25442-39-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,4 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25442-39:
(7*2)+(6*5)+(5*4)+(4*4)+(3*2)+(2*3)+(1*9)=101
101 % 10 = 1
So 25442-39-1 is a valid CAS Registry Number.

25442-39-1Downstream Products

25442-39-1Relevant articles and documents

Thiazolidin-5-imine Formation as a Catalyst-Free Bioorthogonal Reaction for Protein and Live Cell Labeling

Bi, Xiaobao,Yin, Juan,Rao, Chang,Balamkundu, Seetharamsing,Banerjee, Biplab,Zhang, Dingpeng,Zhang, Dawei,Dedon, Peter C.,Liu, Chuan-Fa

, p. 7790 - 7793 (2018)

A previously undescribed reaction involving the formation of a thiazolidin-5-imine linkage was developed for bioconjugation. Being highly specific and operating in aqueous media, this simple condensation reaction is used to chemoselectively label peptides, proteins, and living cells under physiological conditions without the need to use toxic catalysts or reducing reagents.

Prodrugs of compounds that enhance antifungal activity and compositions of said prodrugs

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Page/Page column 65; 66; 67; 74, (2017/05/17)

The invention relates to prodrugs for use in the inhibition of histone deacetylase. The prodrugs of the present invention have good aqueous solubility and good aqueous stability. The prodrugs of the invention advantageously are metabolized to the active i

Prodrugs of Compounds that Enhance Antifungal Activity and Compositions of Said Prodrugs

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Paragraph 0357; 0358; 0372, (2015/07/27)

The invention relates to prodrugs for use in the inhibition of histone deacetylase. The prodrugs of the present invention have good aqueous solubility and good aqueous stability. The prodrugs of the invention advantageously are metabolized to the active i

ANTIANGIOGENIC DRUG TO TREAT CANCER, ARTHRITIS AND RETINOPATHY

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Page/Page column 11, (2010/11/24)

Compounds having Formula (I) or pharmaceutically acceptable salts or prodrugs thereof, are useful for treating pathological states which arise from or are exacerbated by angiogenesis. The invention also relates to pharmaceutical compositions comprising th

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