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67553-36-0

L-Serine, N-(triphenylmethyl)-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 67553-36-0 Structure

  • Basic information

    1. Product Name: L-Serine, N-(triphenylmethyl)-, phenylmethyl ester
    2. Synonyms:
    3. CAS NO:67553-36-0
    4. Molecular Formula: C29H27NO3
    5. Molecular Weight: 437.538
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 67553-36-0.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: L-Serine, N-(triphenylmethyl)-, phenylmethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: L-Serine, N-(triphenylmethyl)-, phenylmethyl ester(67553-36-0)
    11. EPA Substance Registry System: L-Serine, N-(triphenylmethyl)-, phenylmethyl ester(67553-36-0)

  • 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: 67553-36-0(Hazardous Substances Data)

67553-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67553-36-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,5 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67553-36:
(7*6)+(6*7)+(5*5)+(4*5)+(3*3)+(2*3)+(1*6)=150
150 % 10 = 0
So 67553-36-0 is a valid CAS Registry Number.

67553-36-0Relevant articles and documents

Oligo(serine ester) Charge-Altering Releasable Transporters: Organocatalytic Ring-Opening Polymerization and their Use for in Vitro and in Vivo mRNA Delivery

Benner, Nancy L.,McClellan, Rebecca L.,Turlington, Christopher R.,Haabeth, Ole A. W.,Waymouth, Robert M.,Wender, Paul A.

, p. 8416 - 8421 (2019)

RNA technology is transforming life science research and medicine, but many applications are limited by the accessibility, cost, efficacy, and tolerability of delivery systems. Here we report the first members of a new class of dynamic RNA delivery vector

Genetic encoding of 2-aryl-5-carboxytetrazole-based protein photo-cross-linkers

Tian, Yulin,Lin, Qing

supporting information, p. 4449 - 4452 (2018/05/03)

Three γ-heteroatom-substituted N-methylpyrroletetrazole-lysines (mPyTXKs) were synthesized and subsequently incorporated into proteins site-specifically via genetic code expansion. The γ-seleno-substituted derivative, mPyTSeK, showed excellent incorporati

Selective Targeting of the TPX2 Site of Importin-α Using Fragment-Based Ligand Design

Holvey, Rhian S.,Valkov, Eugene,Neal, David,Stewart, Murray,Abell, Chris

supporting information, p. 1232 - 1239 (2015/07/07)

Protein-protein interactions are difficult therapeutic targets, and inhibiting pathologically relevant interactions without disrupting other essential ones presents an additional challenge. Herein we report how this might be achieved for the potential ant

Aziridine ring opening as regio- and stereoselective access to O-glycosyl amino acids and their transformation into O-glycopeptide mimetics

Schaefer, Andreas,Henkensmeier, Dirk,Kroeger, Lars,Thiem, Joachim

body text, p. 902 - 909 (2009/09/25)

Glycosyl amino acid mimetics of the typical GalNAc-(1→O)-Ser/Thr motif of O-glycopeptides were synthesised. Starting from galactose a 1,5-anhydro derivative could be obtained and regio- and stereoselectively coupled to serine- or threonine-derived aziridine compounds, respectively. The corresponding Fmoc derivatives could be used to prepare two 13-mer glycopeptides of the mucin MUC1 carrying instead of Ser-2 or Th-5, the corresponding O-glcycosyl amino acid mimetics.

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