Cas 600709-35-1,L-Alanine, 3-[bis(2,5-dimethylphenyl)phosphinothioyl]-N-[(1,1-dimethylethoxy)carb onyl]-, methyl ester

600709-35-1

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Basic information

Product Name: L-Alanine, 3-[bis(2,5-dimethylphenyl)phosphinothioyl]-N-[(1,1-dimethylethoxy)carb onyl]-, methyl ester
Synonyms:
CAS NO:600709-35-1
Molecular Formula: C25H34NO4PS
Molecular Weight: 475.589
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: L-Alanine, 3-[bis(2,5-dimethylphenyl)phosphinothioyl]-N-[(1,1-dimethylethoxy)carb onyl]-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: L-Alanine, 3-[bis(2,5-dimethylphenyl)phosphinothioyl]-N-[(1,1-dimethylethoxy)carb onyl]-, methyl ester(600709-35-1)
EPA Substance Registry System: L-Alanine, 3-[bis(2,5-dimethylphenyl)phosphinothioyl]-N-[(1,1-dimethylethoxy)carb onyl]-, methyl ester(600709-35-1)

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: 600709-35-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 600709-35-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,0,7,0 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 600709-35:
(8*6)+(7*0)+(6*0)+(5*7)+(4*0)+(3*9)+(2*3)+(1*5)=121
121 % 10 = 1
So 600709-35-1 is a valid CAS Registry Number.

600709-35-1Upstream product

600709-35-1Downstream Products

600709-44-2 3-[bis-(2,5-dimethyl-phenyl)-phosphinothioyl]-2-tert-butoxycarbonylamino-propionic acid

600709-35-1Relevant academic research and scientific papers

High asymmetric induction with β-turn-derived palladium phosphine complexes

Greenfield, Scott J.,Agarkov, Anton,Gilbertson, Scoff R.

, p. 3069 - 3072 (2007/10/03)

(Matrix presented) Work toward the development of a bisphosphine ligand system for the palladium-catalyzed addition to cyclic allyl acetates is reported. A parallel approach using phosphine-containing amino acids in conjunction with natural amino acids wa

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