Cas 1007121-74-5,(S)-3-(benzyloxycarbonyl)-4-isobutyl-[1,2,3]oxathiazolidine 2,2-dioxide

1007121-74-5

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Basic information

Product Name: (S)-3-(benzyloxycarbonyl)-4-isobutyl-[1,2,3]oxathiazolidine 2,2-dioxide
Synonyms: (S)-3-(benzyloxycarbonyl)-4-isobutyl-[1,2,3]oxathiazolidine 2,2-dioxide
CAS NO:1007121-74-5
Molecular Formula:
Molecular Weight: 313.375
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: (S)-3-(benzyloxycarbonyl)-4-isobutyl-[1,2,3]oxathiazolidine 2,2-dioxide(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-(benzyloxycarbonyl)-4-isobutyl-[1,2,3]oxathiazolidine 2,2-dioxide(1007121-74-5)
EPA Substance Registry System: (S)-3-(benzyloxycarbonyl)-4-isobutyl-[1,2,3]oxathiazolidine 2,2-dioxide(1007121-74-5)

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: 1007121-74-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1007121-74-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,1,2 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1007121-74:
(9*1)+(8*0)+(7*0)+(6*7)+(5*1)+(4*2)+(3*1)+(2*7)+(1*4)=85
85 % 10 = 5
So 1007121-74-5 is a valid CAS Registry Number.

1007121-74-5Upstream product

6216-61-1 (S)-(-)-N-(benzyloxycarbonyl)leucinol

1007121-74-5Downstream Products

1007121-80-3 benzyl (S)-1-(N-allyl-4-methylbenzenesulfonamido)-4-methylpentan-2-ylcarbamate

1007121-74-5Relevant academic research and scientific papers

Synthesis of 2,6-disubstituted piperazines by a diastereoselective palladium-catalyzed hydroamination reaction

Cochran, Brian M.,Michael, Forrest E.

, p. 329 - 332 (2008/09/19)

(Chemical Equation Presented) A highly diastereoselective intramolecular hydroamination is the key step in a modular synthesis of 2,6-disubstituted piperazines. The requisite hydroamination substrates were prepared in excellent yields by nucleophilic disp

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