Cas 101020-41-1,(4S,5R)-4-Azidomethyl-5-benzyloxymethyl-2,2,4-trimethyl-[1,3]dioxolane

101020-41-1

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Basic information

Product Name: (4S,5R)-4-Azidomethyl-5-benzyloxymethyl-2,2,4-trimethyl-[1,3]dioxolane
Synonyms:
CAS NO:101020-41-1
Molecular Formula:
Molecular Weight: 291.35
EINECS: N/A
Product Categories: N/A
Mol File: 101020-41-1.mol
Article Data: 1

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: (4S,5R)-4-Azidomethyl-5-benzyloxymethyl-2,2,4-trimethyl-[1,3]dioxolane(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5R)-4-Azidomethyl-5-benzyloxymethyl-2,2,4-trimethyl-[1,3]dioxolane(101020-41-1)
EPA Substance Registry System: (4S,5R)-4-Azidomethyl-5-benzyloxymethyl-2,2,4-trimethyl-[1,3]dioxolane(101020-41-1)

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: 101020-41-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 101020-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,2 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 101020-41:
(8*1)+(7*0)+(6*1)+(5*0)+(4*2)+(3*0)+(2*4)+(1*1)=31
31 % 10 = 1
So 101020-41-1 is a valid CAS Registry Number.

101020-41-1Upstream product

131-11-3 phthalic acid dimethyl ester

101020-41-1Downstream Products

101020-41-1Relevant articles and documents

AN ENANTIOSELECTIVE SYNTHESIS OF THE CARZINOPHILIN DEGRADATION PRODUCT (2S,3S) 4-AMINO-2,3-DIHYDROXY-3-METHYLBUTYRIC ACID

Garner, Philip,Park, Jung Min,Rotello, Vicent

, p. 3299 - 3302 (1985)

An efficient, enantioselective synthesis of (2S,3S) 4-amino-2,3-dihydroxy-3-methylbutyric acid (1) is described.The sequence includes the direct use of azide to selectively open a secondary epoxy alcohol formed under Payne rearrangement conditions.

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