Cas 102727-60-6,(R)-2-Benzyloxy-4-[(4S,6R)-2,2,6-trimethyl-6-(tetrahydro-pyran-2-yloxymethyl)-[1,3]dioxan-4-yl]-butyraldehyde

102727-60-6

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Basic information

Product Name: (R)-2-Benzyloxy-4-[(4S,6R)-2,2,6-trimethyl-6-(tetrahydro-pyran-2-yloxymethyl)-[1,3]dioxan-4-yl]-butyraldehyde
Synonyms:
CAS NO:102727-60-6
Molecular Formula:
Molecular Weight: 420.546
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: (R)-2-Benzyloxy-4-[(4S,6R)-2,2,6-trimethyl-6-(tetrahydro-pyran-2-yloxymethyl)-[1,3]dioxan-4-yl]-butyraldehyde(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-Benzyloxy-4-[(4S,6R)-2,2,6-trimethyl-6-(tetrahydro-pyran-2-yloxymethyl)-[1,3]dioxan-4-yl]-butyraldehyde(102727-60-6)
EPA Substance Registry System: (R)-2-Benzyloxy-4-[(4S,6R)-2,2,6-trimethyl-6-(tetrahydro-pyran-2-yloxymethyl)-[1,3]dioxan-4-yl]-butyraldehyde(102727-60-6)

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: 102727-60-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 102727-60-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,7,2 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 102727-60:
(8*1)+(7*0)+(6*2)+(5*7)+(4*2)+(3*7)+(2*6)+(1*0)=96
96 % 10 = 6
So 102727-60-6 is a valid CAS Registry Number.

102727-60-6Upstream product

102727-60-6Downstream Products

102795-18-6 (3R,8S,9S)-10-Benzenesulfonyl-3-benzyloxy-8-(1-ethoxy-ethoxy)-9-methyl-1-[(4S,6R)-2,2,6-trimethyl-6-(tetrahydro-pyran-2-yloxymethyl)-[1,3]dioxan-4-yl]-dec-5-yn-4-ol

102727-60-6Relevant academic research and scientific papers

Synthetic studies toward marine toxic polyethers. 3. Stereocontrol for segment-A1 of okadaic acid by means of oxymercuration and epoxydation

Isobe,Ichikawa,Goto

, p. 5199 - 5202 (2007/10/02)

Segment-A1 of okadaic acid was synthesized from glucose via an acyclic stereocontrol for C-2 by means of oxymercuration. The stereochemistry was proven by comparison with S and R epoxides which were synthesized selectively by chelational and st

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