Cas 141330-70-3,2,2-Dimethyl-propionic acid (2R,3S,4R,5R,6S)-2-{[(S)-(4-chloro-phenyl)-(diethoxy-phosphoryl)-methyl]-amino}-3,5-bis-(2,2-dimethyl-propionyloxy)-6-methyl-tetrahydro-pyran-4-yl ester

141330-70-3

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Basic information

Product Name: 2,2-Dimethyl-propionic acid (2R,3S,4R,5R,6S)-2-{[(S)-(4-chloro-phenyl)-(diethoxy-phosphoryl)-methyl]-amino}-3,5-bis-(2,2-dimethyl-propionyloxy)-6-methyl-tetrahydro-pyran-4-yl ester
Synonyms:
CAS NO:141330-70-3
Molecular Formula:
Molecular Weight: 676.184
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: 2,2-Dimethyl-propionic acid (2R,3S,4R,5R,6S)-2-{[(S)-(4-chloro-phenyl)-(diethoxy-phosphoryl)-methyl]-amino}-3,5-bis-(2,2-dimethyl-propionyloxy)-6-methyl-tetrahydro-pyran-4-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2,2-Dimethyl-propionic acid (2R,3S,4R,5R,6S)-2-{[(S)-(4-chloro-phenyl)-(diethoxy-phosphoryl)-methyl]-amino}-3,5-bis-(2,2-dimethyl-propionyloxy)-6-methyl-tetrahydro-pyran-4-yl ester(141330-70-3)
EPA Substance Registry System: 2,2-Dimethyl-propionic acid (2R,3S,4R,5R,6S)-2-{[(S)-(4-chloro-phenyl)-(diethoxy-phosphoryl)-methyl]-amino}-3,5-bis-(2,2-dimethyl-propionyloxy)-6-methyl-tetrahydro-pyran-4-yl ester(141330-70-3)

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: 141330-70-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141330-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,3 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141330-70:
(8*1)+(7*4)+(6*1)+(5*3)+(4*3)+(3*0)+(2*7)+(1*0)=83
83 % 10 = 3
So 141330-70-3 is a valid CAS Registry Number.

141330-70-3Upstream product

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141330-70-3Relevant academic research and scientific papers

Carbohydrates as chiral templates: Stereoselective synthesis of (R)- and (S)-α-aminophosphonic acid derivatives

Laschat,Kunz

, p. 90 - 95 (2007/10/02)

The stereoselective synthesis of diethyl (S)- or (R)-α-[(O-pivaloyl-hexapyranosyl)amino]benzylphosphonates is achieved via Lewis acid catalyzed addition of diethyl phosphite to O-pivaloylated N-benzylidene-β-D-galactosylamine or N-benzylidene-α-D-arabinop

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