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(-)-Oppositol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50906-52-0

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50906-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50906-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,9,0 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 50906-52:
(7*5)+(6*0)+(5*9)+(4*0)+(3*6)+(2*5)+(1*2)=110
110 % 10 = 0
So 50906-52-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H25BrO/c1-10(2)9-11-5-7-14(3)12(16)6-8-15(4,17)13(11)14/h9,11-13,17H,5-8H2,1-4H3/t11-,12-,13-,14+,15+/m0/s1

50906-52-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,3aS,4R,7S,7aS)-7-bromo-4,7a-dimethyl-3-(2-methylprop-1-enyl)-2,3,3a,5,6,7-hexahydro-1H-inden-4-ol

1.2 Other means of identification

Product number -
Other names Oppositol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:50906-52-0 SDS

50906-52-0Downstream Products

50906-52-0Relevant articles and documents

A stereoselective total synthesis of (±)-oppositol by a doubly diastereoselective intramolecular ester enolate alkylation

Kim, Deukjoon,Kim, In Ho

, p. 415 - 416 (2007/10/03)

The brominated terpene (±)-oppositol (1) has been synthesized utilizing a novel doubly diastereodifferentialing 'folding and allylic strain-controlled' intramolecular ester enolate alkylation.

SYNTHESIS OF (+/-)-PREPINNATERPENE, A BROMODITERPENE FROM THE RED ALGA LAURENCIA PINNATA YAMADA

Fukuzawa, Akio,Sato, Hideaki,Masamune, Tadashi

, p. 4303 - 4306 (2007/10/02)

A total synthesis of (+/-)-prepinnaterpene, a brominated diterpene with a unique skeleton, and (+/-)-oppositol, a related sesquiterpene, is described.

BIOMIMETIC SYNTHESES OF OPPOSITOL, OPLOPANONE, AND APHANAMOL II FROM GERMACRENE-D

Shizuri, Yoshikazu,Shu, Yamaguchi,Terada, Yukimasa,Yamamura, Shosuke

, p. 57 - 60 (2007/10/02)

Biomimetic reaction of germacrene-D induced with bromonium ion has been carried out to give several bromo compounds, from which (+/-)-oppositol and (+/-)-oplopanone have been synthesized. (+/-)-Aphanamol II has also been synthesized from epoxygermacrene-D.

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