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19781-52-3

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19781-52-3 Usage

Synthesis Reference(s)

Synthesis, p. 283, 1989Tetrahedron Letters, 17, p. 1295, 1976 DOI: 10.1016/S0040-4039(00)78044-0

Check Digit Verification of cas no

The CAS Registry Mumber 19781-52-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,8 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19781-52:
(7*1)+(6*9)+(5*7)+(4*8)+(3*1)+(2*5)+(1*2)=143
143 % 10 = 3
So 19781-52-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O/c1-5-6(2)7(3,4)8/h5,8H,1-4H3/b6-5+

19781-52-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-DIMETHYL-4-PENTEN-2-OL

1.2 Other means of identification

Product number -
Other names 2,3-dimethyl-pent-4-en-2-ol

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:19781-52-3 SDS

19781-52-3Relevant articles and documents

-

Zurqiyah,A.,Castro,C.E.

, p. 1504 - 1506 (1969)

-

Highly efficient synthesis of the tricyclic core of taxol by cascade metathesis

Letort, Aurelien,Aouzal, Remi,Ma, Cong,Long, De-Liang,Prunet, Joelle

supporting information, p. 3300 - 3303 (2014/07/08)

An efficient enantioselective synthesis of the ABC tricyclic core of the anticancer drug Taxol is reported. The key step of this synthesis is a cascade metathesis reaction, which leads in one operation to the required tricycle if appropriate fine-tuning o

On the Regioselectivity of Coupling of Substituted Allyl Radicals. Steric Versus FMO Control

Pasto, Daniel J.,L'Hermine, Gael

, p. 3259 - 3272 (2007/10/02)

The photo-induced decomposition of substituted-homoallylic 4-nitrobenzenesulfenates produces substituted allyl radicals which undergo dimerization and coupling with the 4-nitrobenzenethiyl radical.The regioselectivity of the dimerization of the allyl redi

ELECTROSYNTHESIS OF ALCOHOLS FROM ORGANIC HALIDES AND KETONES OR ALDEHYDES

Sibille, Soline,d'Incan, Esther,Leport, Louis,Perichon, Jacques

, p. 3129 - 3132 (2007/10/02)

The electrosynthesis of a wide range of alcohols from organic halides and ketones or aldehydes is achieved under simple and mild conditions in an undivided electrolytic cell using different sacrificial anodes.

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