Cas 149730-90-5,(3aR,6S,6aR)-6-Benzyloxymethyl-4-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ol

149730-90-5

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Basic information

Product Name: (3aR,6S,6aR)-6-Benzyloxymethyl-4-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ol
Synonyms:
CAS NO:149730-90-5
Molecular Formula:
Molecular Weight: 310.347
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: (3aR,6S,6aR)-6-Benzyloxymethyl-4-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ol(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,6S,6aR)-6-Benzyloxymethyl-4-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ol(149730-90-5)
EPA Substance Registry System: (3aR,6S,6aR)-6-Benzyloxymethyl-4-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ol(149730-90-5)

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: 149730-90-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 149730-90-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,7,3 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 149730-90:
(8*1)+(7*4)+(6*9)+(5*7)+(4*3)+(3*0)+(2*9)+(1*0)=155
155 % 10 = 5
So 149730-90-5 is a valid CAS Registry Number.

149730-90-5Upstream product

77-76-9 2,2-dimethoxy-propane

149730-90-5Downstream Products

83289-84-3 C₁₉H₂₆O₆

149730-90-5Relevant academic research and scientific papers

THE STEREOSELECTIVE SYNTHESIS OF L-TAGATOSE. AN APPLICATION OF Zn(II) MEDIATED HIGHLY STEREOSELECTIVE ADDITION OF 2-FURYLLITHIUM TO POLYOXYGENATED ALDEHYDE

Mukaiyama, Teruaki,Yuki, Yoichi,Suzuki, Keisuke

, p. 1169 - 1170 (1982)

In the presence of ZnBr2, the addition of 2-furyllithium to 4-O-benzyl-2,3-O-isopropylidene-L-threose proceeded in a highly stereoselective manner to afford the anti-adduct, which was further converted to L-tagatose.

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