Cas 96239-87-1,Toluene-4-sulfonic acid (3R,6R,9R,10S)-9-benzyloxymethyl-10-hydroxy-1,7-dioxa-spiro[5.5]undec-3-ylmethyl ester

96239-87-1

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Basic information

Product Name: Toluene-4-sulfonic acid (3R,6R,9R,10S)-9-benzyloxymethyl-10-hydroxy-1,7-dioxa-spiro[5.5]undec-3-ylmethyl ester
Synonyms: Toluene-4-sulfonic acid (3R,6R,9R,10S)-9-benzyloxymethyl-10-hydroxy-1,7-dioxa-spiro[5.5]undec-3-ylmethyl ester
CAS NO:96239-87-1
Molecular Formula:
Molecular Weight: 476.591
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: Toluene-4-sulfonic acid (3R,6R,9R,10S)-9-benzyloxymethyl-10-hydroxy-1,7-dioxa-spiro[5.5]undec-3-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Toluene-4-sulfonic acid (3R,6R,9R,10S)-9-benzyloxymethyl-10-hydroxy-1,7-dioxa-spiro[5.5]undec-3-ylmethyl ester(96239-87-1)
EPA Substance Registry System: Toluene-4-sulfonic acid (3R,6R,9R,10S)-9-benzyloxymethyl-10-hydroxy-1,7-dioxa-spiro[5.5]undec-3-ylmethyl ester(96239-87-1)

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: 96239-87-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 96239-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,3 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 96239-87:
(7*9)+(6*6)+(5*2)+(4*3)+(3*9)+(2*8)+(1*7)=171
171 % 10 = 1
So 96239-87-1 is a valid CAS Registry Number.

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96239-87-1Relevant academic research and scientific papers

DIASTEREOTOPIC SELECTIVITY AT PROCHIRAL CARBON CENTERS. A STEREODIVERGENT SYNTHESIS OF THE TALAROMYCINS.

Schreiber, Stuart L.,Sommer, Toby J.,Satake, Kunio

, p. 17 - 20 (1985)

The transformation of the acyclic precursor previously employed in the synthesis of talaromycin B to the stereoisomeric avian toxin talaromycin A is described.Diastereotopic selectivity at prochiral carbon centers in an acetonide migration and in a subseq

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