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3,3-dimethylbicyclo[2.2.1]heptane-2-methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27899-45-2

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27899-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27899-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,8,9 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27899-45:
(7*2)+(6*7)+(5*8)+(4*9)+(3*9)+(2*4)+(1*5)=172
172 % 10 = 2
So 27899-45-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-10(2)8-4-3-7(5-8)9(10)6-11/h7-9,11H,3-6H2,1-2H3

27899-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2.2-Dimethyl-3-oxymethyl-bicyclo-[1.2.2]-heptan

1.2 Other means of identification

Product number -
Other names (3,3-Dimethyl-bicyclo[2.2.1]hept-2-yl)-methanol

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:27899-45-2 SDS

27899-45-2Relevant academic research and scientific papers

A General Regioselective Synthesis of Alcohols by Cobalt-Catalyzed Hydrogenation of Epoxides

Beller, Matthias,Junge, Kathrin,Leischner, Thomas,Li, Wu,Liu, Weiping

supporting information, p. 11321 - 11324 (2020/05/16)

A straightforward methodology for the synthesis of anti-Markovnikov-type alcohols is presented. By using a specific cobalt triphos complex in the presence of Zn(OTf)2 as an additive, the hydrogenation of epoxides proceeds with high yields and selectivities. The described protocol shows a broad substrate scope, including multi-substituted internal and terminal epoxides, as well as a good functional-group tolerance. Various natural-product derivatives, including steroids, terpenoids, and sesquiterpenoids, gave access to the corresponding alcohols in moderate-to-excellent yields.

Preparation of polyfunctional phosphines using zinc organometallics

Langer, Falk,Puentener, Kurt,Stuermer, Rainer,Knochel, Paul

, p. 715 - 738 (2007/10/03)

The reaction of functionalized diorganozincs with chlorodiorganophosphines provides polyfunctional phosphines in good yields. Especially attractive is the hydroboration/boron-zinc exchange sequence which allows the conversion of functionalized olefins into polyfunctional phosphines in a one-pot procedure. Several new chiral phosphines have been prepared starting from readily available chiral olefins (terpenes) and their efficiency in asymmetric hydrogenation reactions has been evaluated.

Novel Reduction of Carboxylic Acids and Hydroboration of Olefins by Electrolysis of Sodium Borohydride

Shundo, Ryushi,Matsubara, Yoshiharu,Nishiguchi, Ikuzo,Hirashima, Tsuneaki

, p. 530 - 534 (2007/10/02)

Electrochemical oxidation of sodium borohydride in diglyme containing aliphatic or aromatic carboxylic acids followed by acid-catalyzed hydrolysis afforded the corresponding primary alcohols in good yields.Furthermore, similar electrochemical oxidation in the presence of a variety of olefins instead of carboxylic acids, followed by treatment with alkaline-hydrogen peroxide, brought about novel electrochemical hydroboration to give the corresponding alcohols regio- and stereoselectively in good yields.

A Facile Conversion of Alkenes to Alcohols with Benzyltriethylammonium Borohydride-Chlorotrimethylsilane

Baskaran, Sundarababu,Gupta, Varsha,Chidambaram, Nallaperumal,Chandrasekaran, Srinivasan

, p. 903 - 904 (2007/10/02)

A combination of benzyltrimethylammonium borohydride and chlorotrimethylsilane (1:1) in dichloromethane at 0 deg C has been found to be a convenient reagent system for the conversion of alkenes to alcohols, the hydroxy group of which is introduced in an anti-Markovnikov manner.

Oxygenation of Oleefinic Hydrocarbons Catalyzed by Iron(II) Acetonitrile Solvate

Kobayashi, Shigeki,Kotani, Eiichi,Ishii, Yoko,Tobinaga, Seisho

, p. 610 - 614 (2007/10/02)

Oxygenation reactions of olefins having an endo- or exo-cyclic double bond, namely, cyclohexene, norbornene, camphene, longifolene, and ent-kaurene, with a simple model reagent, Fe(MeCN)62+-H2O2-Ac2O, for mono-oxygenase were investigated in connection with their biotransformations.Keywords oxygenation; olefin; endo-cyclic double bond; exo-cyclic double bond; iron(II) acetonitrile solvate; hydrogen peroxide; model enzyme; mono-oxygenase

Novel Method for Hydroboration of Olefins Using Electrolysis

Shundo, Ryushi,Matsubara, Yoshiharu,Nishiguchi, Ikuzo,Hirashima, Tsuneaki

, p. 2033 - 2036 (2007/10/02)

A first example of electrochemical hydroboration of olefins was found.Anodic oxidation of sodium borohydride in the presence of olefins in diglyme followed by conventional oxidation gave the corresponding alcohols regio- and stereoselectively in good yields.

A Convenient One-pot Hydroboration / Isomerization / Oxidation of Longifolene to Isolongifolol

Vyas, Pramod,Nayak, U. R.

, p. 337 - 339 (2007/10/02)

A convenient one-pot hydroboration / isomerization / oxidation of longifolene (1) to the thermodynamically more stable epimer, isolongifolol (3) is described.Furthermore, a practical in situ method for the hydroboration of 1 in THF, has been optimised to generate the less stable epimer, longifolol (2).

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