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(2R,6S,8R,9R)-4,8-dibromo-9-chloro-2,5,5,9-tetramethylspiro[5.5]undec-3-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72036-07-8

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72036-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72036-07-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,3 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 72036-07:
(7*7)+(6*2)+(5*0)+(4*3)+(3*6)+(2*0)+(1*7)=98
98 % 10 = 8
So 72036-07-8 is a valid CAS Registry Number.

72036-07-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,6S,9R,10R)-4,10-dibromo-9-chloro-2,5,5,9-tetramethylspiro[5.5]undec-3-en-1-one

1.2 Other means of identification

Product number -
Other names Spiro(5.5)undec-3-en-1-one,4,8-dibromo-9-chloro-2,5,5,9-tetramethyl-,(2R,6S,8R,9R)-rel-(+)

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:72036-07-8 SDS

72036-07-8Upstream product

72036-07-8Downstream Products

72036-07-8Relevant academic research and scientific papers

Kylinone, a New Sesquiterpene Skeleton from the Marine Alga Laurencia pacifica

Selover, Scott J.,Crews, Phillip

, p. 69 - 72 (1980)

The structure of a new spirobicycloundecane sesquiterpene, kylinone (1), is reported.The relative configurations at all four chiral centers have been assigned as 3S*, 4S*, 6R* and 8S* on the basis of a combination of spectroscopic and chemical observation.Kylinone (1) has been synthesized from a known chamigrene, deoxyprepacifenol (7), by epoxide opening accompanied by a methyl migration.Epoxide openings in the other related spirocyclic undecanes 8 and 10 are also discussed.

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