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130790-60-2

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130790-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130790-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,7,9 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 130790-60:
(8*1)+(7*3)+(6*0)+(5*7)+(4*9)+(3*0)+(2*6)+(1*0)=112
112 % 10 = 2
So 130790-60-2 is a valid CAS Registry Number.

130790-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E,6R)-1-benzyloxy-3,7-dimethyl-2-octene-6,7-diol

1.2 Other means of identification

Product number -
Other names (R,E)-8-benzyloxy-2,6-dimethyloct-6-ene-2,3-diol

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:130790-60-2 SDS

130790-60-2Relevant articles and documents

Oxidative cyclization of diols derived from 1,5-dienes: Formation of enantiopure cis-tetrahydrofurans by using catalytic osmium tetroxide; formal synthesis of (+)-cis-solamin

Donohoe, Timothy J.,Butterworth, Sam

, p. 4766 - 4768 (2007/10/03)

(Chemical Equation Presented) High yields and high levels of stereocontrol are observed in the oxidative cyclization of vicinal diols using catalytic amounts of a transition metal (see scheme; TFA = trifluoroacetic acid). The product stereochemistry is co

Total synthesis of (+)-curacin A, a marine cytotoxic agent

Hoemann, Michael Z.,Agrios, Konstantinos A.,Aube, Jeffrey

, p. 11087 - 11098 (2007/10/03)

The total synthesis of curacin A, a cytotoxic agent that interacts with the colchicine binding site on tubulin, is described. The convergent synthesis utilizes natural product and chiral pool starting materials (geraniol, serine) and asymmetric synthesis

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