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bicyclo[3.1.1]heptan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17159-87-4

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17159-87-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17159-87-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,5 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17159-87:
(7*1)+(6*7)+(5*1)+(4*5)+(3*9)+(2*8)+(1*7)=124
124 % 10 = 4
So 17159-87-4 is a valid CAS Registry Number.

17159-87-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name bicyclo[3.1.1]heptan-4-one

1.2 Other means of identification

Product number -
Other names 2-Oxobicyclo<3.1.1>heptan

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:17159-87-4 SDS

17159-87-4Relevant academic research and scientific papers

COMPOUNDS FOR THE TREATMENT OF HIV

-

, (2013/03/26)

The invention provides compounds of formula (I): or a salt thereof as described herein. The invention also provides pharmaceutical compositions comprising a compound of formula (I), processes for preparing compounds of formula (I), intermediates useful for preparing compounds of formula I and therapeutic methods for treating a Retroviridae viral infection including an infection caused by the HIV virus.

A New Synthesis of Bicycloocta-2,4-diene and Its Cycloaddition Reactions with Dienophiles.

Yin, Tyze-Kuan,Lee, Jon Gun,Borden, Weston Thatcher

, p. 531 - 534 (2007/10/02)

Bicycloocta-2,4-diene (4) has been synthesized by a new, nine-step route, starting from 2--1,3-butadiene and acrolein.Diene (4) proved almost as unreactive toward Diels-Alder cycloadditions as the previously studied 7,7-dimethy

SYNTHESIS OF THROMBOXANE A2 ANALOGS-1. (+/-)-DIMETHANOTHROMBOXANE A2

Ohuchida, Shuichi,Hamanaka, Nobuyuki,Hayashi, Masaki

, p. 4257 - 4262 (2007/10/02)

The stable thromboxane A2 analog (+/-)-dimethanothromboxane A2 1 was synthesized from bicycloheptane 2 via the tricyclic compound 4.

Regioselectivity in Ring-Expansion of 1-Substituted Bicyclohexan-2-ones: Preferential Migration of Methylene Over Bridgehead Carbon

Della, Ernest W.,Pigou, Paul E.

, p. 2261 - 2268 (2007/10/02)

Ring expansion of several 1-substituted bicyclohexan-2-ones has been investigated in order to compare the effect od substitution on the migratory aptitude of the bridgehead carbon in relation to the methylene carbon.In the cases examined it was observed that there is a marked preference for migration of the methylene carbon, with the substituted substrates displaying higher regioselectivity that the parent ketone.In the rearrangement of both 1-fluoro- and 1-chloro-bicyclohexan-2-one, migration of the methylene carbon occurs exclusively.

A FACILE SYNTHESIS OF 2-FORMYLBICYCLOHEPT-2-ENE

Cooper, G. F.,VanHorn, A. R.,Wren, D.

, p. 1213 - 1218 (2007/10/02)

A short synthesis of 2-formylbicyclohept-2-ene, suitable for multigram preparations, is presented.

Deamination Reactions. 35. Decomposition of 5-Norbornene-2-diazonium Ions. Derivatives of Bicyclohept-2-ene

Kirmse, Wolfgang,Knoepfel, Norbert,Loosen, Karin,Siegfried, Rainer,Wroblowsky, Heinz-Juergen

, p. 1187 - 1191 (2007/10/02)

Photolysis of 5-norbornen-2-one tosylhydrazone (4) in aqueous sodium hydroxide afforded 4percent of 3-norpinen-2-ol (3) in addition to 5-norbornen-2-ol (5, 10percent) and nortricyclanol (6, 86percent). 3 arises from 5-norbornene-2endo-diazonium ions (2) as shown by the nitrous acid deamination of the epimeric amines 1 and 7. 3-Norpinen-2-one (12) was isolated by oxidation of the deamination products followed by preparative g.l.c. 3 and 12 were synthesized independently from norpinan-2-one (9) via sulfenylation and sulfoxide pyrolysis.The norbornene -> norpinene rearrangement is slightly enhanced by 1-OCH3.The deamination of 1-methoxy-5-norbornen-2endo-amine (14) produced 10percent of 12, as compared to 5.6percent of 3 from 1.

Carbocyclic thromboxane A2 analogues

-

, (2008/06/13)

Stable biologically active thromboxane A2 analogues having the formula: STR1 wherein R1 is OR3, where R3 represents hydrogen or a pharmaceutically acceptable cation or lower alkyl group; or R1 is NR4 R5 where R4 and R5 are the same or different substituents selected from the group consisting of hydrogen and lower alkyl group; and R2 is hydrogen or an --OH group. The thromboxane analogues are potent thrombotic agents, useful in cardiovascular treatment.

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