Cas 151371-10-7,D-(-)-threo-1-(p-nitrophenyl)-2-(N-tritylglycylamido)-1,3-propanediol

151371-10-7

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Basic information

Product Name: D-(-)-threo-1-(p-nitrophenyl)-2-(N-tritylglycylamido)-1,3-propanediol
Synonyms: D-(-)-threo-1-(p-nitrophenyl)-2-(N-tritylglycylamido)-1,3-propanediol
CAS NO:151371-10-7
Molecular Formula:
Molecular Weight: 511.577
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: D-(-)-threo-1-(p-nitrophenyl)-2-(N-tritylglycylamido)-1,3-propanediol(CAS DataBase Reference)
NIST Chemistry Reference: D-(-)-threo-1-(p-nitrophenyl)-2-(N-tritylglycylamido)-1,3-propanediol(151371-10-7)
EPA Substance Registry System: D-(-)-threo-1-(p-nitrophenyl)-2-(N-tritylglycylamido)-1,3-propanediol(151371-10-7)

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: 151371-10-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 151371-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,3,7 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 151371-10:
(8*1)+(7*5)+(6*1)+(5*3)+(4*7)+(3*1)+(2*1)+(1*0)=97
97 % 10 = 7
So 151371-10-7 is a valid CAS Registry Number.

151371-10-7Upstream product

151371-10-7Downstream Products

13215-27-5 D-(-)-threo-1-(p-nitrophenyl)-2-(glycylamido)-1,3-propanediol

151371-10-7Relevant academic research and scientific papers

Aminoacyl analogs of chloramphenicol: Examination of the kinetics of inhibition of peptide bond formation

Drainas,Mamos,Coutsogeorgopoulos

, p. 3542 - 3545 (1993)

Two aminoacyl analogs and one peptidyl analog of chloramphenicol (1, Cl2CHCO-CA) were prepared. These are 2 (L-Phe-CA), 3 (Gly-CA), and 4 (L- Phe-Gly-CA). The kinetics of inhibition of peptide bond formation by these analogs were examined in a

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