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78843-64-8

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78843-64-8 Usage

General Description

(R)-(+)-1,2-HEPTANEDIOL is a chiral compound that consists of a heptane backbone with two hydroxyl groups attached at the 1 and 2 positions. It is commonly used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and fragrances. (R)-(+)-1,2-HEPTANEDIOL is known for its ability to influence the enantioselectivity of reactions, making it a valuable tool in the production of optically pure compounds. In addition, (R)-(+)-1,2-HEPTANEDIOL has been studied for its antimicrobial and antifungal properties, making it a versatile and important chemical in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 78843-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,4 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78843-64:
(7*7)+(6*8)+(5*8)+(4*4)+(3*3)+(2*6)+(1*4)=178
178 % 10 = 8
So 78843-64-8 is a valid CAS Registry Number.

78843-64-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-heptane-1,2-diol

1.2 Other means of identification

Product number -
Other names 1,2-heptanediol

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:78843-64-8 SDS

78843-64-8Downstream Products

78843-64-8Relevant articles and documents

An enantioselective approach to 2-alkyl substituted tetrahydroquinolines: Total synthesis of (+)-angustureine

Garg, Yuvraj,Gahalawat, Suraksha,Pandey, Satyendra Kumar

, p. 38846 - 38850 (2015/05/20)

A simple and highly efficient synthetic approach to enantiopure 2-alkyl substituted tetrahydroquinoline 1 skeleton from aldehydes as starting materials and its application to the total synthesis of (+)-angustureine 2 is described. Key transformations incl

Synthesis of substituted α,β-unsaturated δ-lactones from vinyl tellurides

Oliveira, Juliana M.,R. Freitas, Juliano C.,Comasseto, Jo?o Valdir,Menezes, Paulo Henrique

experimental part, p. 3003 - 3009 (2011/04/27)

A new approach for the synthesis of α,β-unsaturated δ-lactones, a unit present in many natural products with interesting biological activities is described. The approach was based on the use of a vinyl telluride, and it is complementary to the methods usi

A route to 1,2-diols by enantioselective organocatalytic α-oxidation with molecular oxygen

Ibrahem, Ismail,Zhao, Gui-Ling,Sundén, Henrik,Córdova, Armando

, p. 4659 - 4663 (2007/10/03)

A route to 1,2-diols by the direct organocatalytic enantioselective α-oxidation of aldehydes using molecular oxygen is presented. Protected commercially available chiral pyrrolidines catalyze the asymmetric α-oxidation of aldehydes with singlet molecular oxygen with high enantioselectivity to furnish the corresponding diols after in situ reduction in high yield with up to 98% ee. Electrophilic singlet molecular oxygen was photo or chemically generated ('dark' 1O2).

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