Cas 615541-10-1,Benzoic acid (2S,3aR,5S,6S,7R,7aR)-7-benzyloxy-2-methoxy-2,5-dimethyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-6-yl ester

615541-10-1

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Basic information

Product Name: Benzoic acid (2S,3aR,5S,6S,7R,7aR)-7-benzyloxy-2-methoxy-2,5-dimethyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-6-yl ester
Synonyms: Benzoic acid (2S,3aR,5S,6S,7R,7aR)-7-benzyloxy-2-methoxy-2,5-dimethyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-6-yl ester
CAS NO:615541-10-1
Molecular Formula:
Molecular Weight: 414.455
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: Benzoic acid (2S,3aR,5S,6S,7R,7aR)-7-benzyloxy-2-methoxy-2,5-dimethyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-6-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (2S,3aR,5S,6S,7R,7aR)-7-benzyloxy-2-methoxy-2,5-dimethyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-6-yl ester(615541-10-1)
EPA Substance Registry System: Benzoic acid (2S,3aR,5S,6S,7R,7aR)-7-benzyloxy-2-methoxy-2,5-dimethyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-6-yl ester(615541-10-1)

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: 615541-10-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 615541-10-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,5,5,4 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 615541-10:
(8*6)+(7*1)+(6*5)+(5*5)+(4*4)+(3*1)+(2*1)+(1*0)=131
131 % 10 = 1
So 615541-10-1 is a valid CAS Registry Number.

615541-10-1Upstream product

615541-10-1Downstream Products

615541-10-1Relevant academic research and scientific papers

Efficient generation of β-L-rhamnosidic linkages via the ulosyl bromide approach

Lichtenthaler, Frieder W.,Metz, Thomas W.

, p. 5477 - 5480 (1997)

Practical protocols have been developed for the acquisition of ulosyl bromides of type III from L-rhamnose, i.e. 6-deoxy-α-L-arabino-2-ketohexosyl bromides 6-8. They have high potential as indirect β-L-rhamnosyl donors, as they undergo β-specific glycosid

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