Cas 252202-20-3,3-[(3R,4R)-3-tert-Butoxycarbonylamino-4-(2-trimethylsilanyl-ethoxycarbonylamino)-pyrrolidine-1-carbonyl]-benzoic acid

252202-20-3

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Basic information

Product Name: 3-[(3R,4R)-3-tert-Butoxycarbonylamino-4-(2-trimethylsilanyl-ethoxycarbonylamino)-pyrrolidine-1-carbonyl]-benzoic acid
Synonyms:
CAS NO:252202-20-3
Molecular Formula:
Molecular Weight: 493.632
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-[(3R,4R)-3-tert-Butoxycarbonylamino-4-(2-trimethylsilanyl-ethoxycarbonylamino)-pyrrolidine-1-carbonyl]-benzoic acid(CAS DataBase Reference)
NIST Chemistry Reference: 3-[(3R,4R)-3-tert-Butoxycarbonylamino-4-(2-trimethylsilanyl-ethoxycarbonylamino)-pyrrolidine-1-carbonyl]-benzoic acid(252202-20-3)
EPA Substance Registry System: 3-[(3R,4R)-3-tert-Butoxycarbonylamino-4-(2-trimethylsilanyl-ethoxycarbonylamino)-pyrrolidine-1-carbonyl]-benzoic acid(252202-20-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 252202-20-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 252202-20-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,2,0 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 252202-20:
(8*2)+(7*5)+(6*2)+(5*2)+(4*0)+(3*2)+(2*2)+(1*0)=83
83 % 10 = 3
So 252202-20-3 is a valid CAS Registry Number.

252202-20-3Upstream product

252202-20-3Downstream Products

252202-20-3Relevant academic research and scientific papers

Construction of sequence-selective peptide receptors from conformationally restricted eta- and theta-amino acids

Ryan, Kevin,Still, W. Clark

, p. 2673 - 2678 (2007/10/03)

Oligomeric chemoreceptors for tripeptides have been constructed from a set of novel eta- and theta-amino acids. Screening against an encoded combinatorial tripeptide library has revealed two new small molecule chemoreceptor motifs with highly sequence-selective binding properties.

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