Cas 185312-46-3,Benzoic acid (3aR,6S,6aR)-6-bromo-2,2-dimethyl-dihydro-furo[3,4-d][1,3]dioxol-3a-ylmethyl ester

185312-46-3

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Basic information

Product Name: Benzoic acid (3aR,6S,6aR)-6-bromo-2,2-dimethyl-dihydro-furo[3,4-d][1,3]dioxol-3a-ylmethyl ester
Synonyms: Benzoic acid (3aR,6S,6aR)-6-bromo-2,2-dimethyl-dihydro-furo[3,4-d][1,3]dioxol-3a-ylmethyl ester
CAS NO:185312-46-3
Molecular Formula:
Molecular Weight: 357.201
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 (3aR,6S,6aR)-6-bromo-2,2-dimethyl-dihydro-furo[3,4-d][1,3]dioxol-3a-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (3aR,6S,6aR)-6-bromo-2,2-dimethyl-dihydro-furo[3,4-d][1,3]dioxol-3a-ylmethyl ester(185312-46-3)
EPA Substance Registry System: Benzoic acid (3aR,6S,6aR)-6-bromo-2,2-dimethyl-dihydro-furo[3,4-d][1,3]dioxol-3a-ylmethyl ester(185312-46-3)

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: 185312-46-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 185312-46-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,3,1 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 185312-46:
(8*1)+(7*8)+(6*5)+(5*3)+(4*1)+(3*2)+(2*4)+(1*6)=133
133 % 10 = 3
So 185312-46-3 is a valid CAS Registry Number.

185312-46-3Upstream product

185312-46-3Downstream Products

185312-46-3Relevant academic research and scientific papers

Addition of an apiosyl radical to activated olefins - Synthesis of C-apiosyl compounds

Drescher, Martina,Hammerschmidt, Friedrich

, p. 1451 - 1454 (1996)

3'-O-Benzoyl-2,3-O-isopropylidene-D-apio-β-D-furanosyl bromide (8), prepared in two steps from 2,3-O-isopropylidene-D-apio-β-D-furanose (6), was reacted with tris(trimethylsilyl)silane/AIBN in the presence of an excess of a variety of activated olefins such as dimethyl maleate, methyl acrylate, acrylonitrile, methyl vinyl ketone, crotonaldehyde, cyclopent-2-enone, and cyclohex-2-enone to afford the corresponding C-apiosides 10 having β-configuration.

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