Cas 1038433-22-5,3,6-anhydro-2-azido-N,N-diethyl-4,5-O-isopropylidene-7-O-trityl-L-glycero-D-allo-heptonamide

1038433-22-5

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Basic information

Product Name: 3,6-anhydro-2-azido-N,N-diethyl-4,5-O-isopropylidene-7-O-trityl-L-glycero-D-allo-heptonamide
Synonyms: 3,6-anhydro-2-azido-N,N-diethyl-4,5-O-isopropylidene-7-O-trityl-L-glycero-D-allo-heptonamide
CAS NO:1038433-22-5
Molecular Formula:
Molecular Weight: 570.689
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: 3,6-anhydro-2-azido-N,N-diethyl-4,5-O-isopropylidene-7-O-trityl-L-glycero-D-allo-heptonamide(CAS DataBase Reference)
NIST Chemistry Reference: 3,6-anhydro-2-azido-N,N-diethyl-4,5-O-isopropylidene-7-O-trityl-L-glycero-D-allo-heptonamide(1038433-22-5)
EPA Substance Registry System: 3,6-anhydro-2-azido-N,N-diethyl-4,5-O-isopropylidene-7-O-trityl-L-glycero-D-allo-heptonamide(1038433-22-5)

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: 1038433-22-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1038433-22-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,8,4,3 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1038433-22:
(9*1)+(8*0)+(7*3)+(6*8)+(5*4)+(4*3)+(3*3)+(2*2)+(1*2)=125
125 % 10 = 5
So 1038433-22-5 is a valid CAS Registry Number.

1038433-22-5Upstream product

934271-05-3 C₄₃H₆₁ClN₄O₈SSi

1038433-22-5Downstream Products

1038433-22-5Relevant academic research and scientific papers

Studies on reactivity of azidoamides, intermediates in the synthesis of tetrahydroxypipecolic acid derivatives

Pino-Gonzalez, M.-Soledad,Assiego, Carmen,Ona, Noe

, p. 932 - 937 (2008/09/21)

Azido group reduction was observed by the treatment of a 2-azido-3-triisopropylsilyloxy heptonamide derivative with NaI in DMSO. The process allowed us to obtain a tetrahydroxypipecolic acid amide derivative. The same azido amide was treated with LiCl in DMSO, but desilylation occurred to give 3,6-anhydro-2-azido heptonamide.

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