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58931-16-1

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58931-16-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58931-16-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,3 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58931-16:
(7*5)+(6*8)+(5*9)+(4*3)+(3*1)+(2*1)+(1*6)=151
151 % 10 = 1
So 58931-16-1 is a valid CAS Registry Number.

58931-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-1-(benzyloxy)-2-hydroxypent-4-ene

1.2 Other means of identification

Product number -
Other names (+)-(2R)-1-benzyloxy-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:58931-16-1 SDS

58931-16-1Relevant articles and documents

2-THIENYL(CYANO)COPPER LITHIUM. A LOWER ORDER, STABLE "CUPRATE IN A BOTTLE" PRECURSOR TO HIGHER ORDER REAGENTS

Lipshutz, Bruce H.,Koerner, Mike,Parker, David A.

, p. 945 - 948 (1987)

The lower order mixed cuprate derived from CuCN and 2-lithiothiophene (i.e.,2-ThCu(CN)Li) is found to have excellent shelf life, thereby providing an easily formed yet itself unreactive precursor to higher order mixed organocuprates.

Stereoselective total synthesis of (?)-galantinic acid and 1-deoxy-5-hydroxysphingolipids via prins cyclization

Rahman, Md. Ataur,Haque, Ashanul,Yadav, Jhillu Singh

supporting information, (2020/07/03)

The stereoselective total synthesis of (?)-galantinic acid 1 and 1-deoxy-5-hydroxysphingolipids 4 is described via Prins cyclization protocol followed by reductive ring opening sequence of substituted pyrenol derivative 6. The target molecules were synthesized using a common synthetic intermediate epoxide 5. Besides, we also proposed synthetic pathways to achieve other structural analogues using common intermediates.

Bi(cyclopentyl)diol-Derived Boronates in Highly Enantioselective Chiral Phosphoric Acid-Catalyzed Allylation, Propargylation, and Crotylation of Aldehydes

Yuan, Jinping,Jain, Pankaj,Antilla, Jon C.

, p. 12988 - 13003 (2020/11/23)

In this study, we disclose the catalytic addition of bi(cyclopentyl)diol-derived boronates to aldehydes promoted by chiral phosphoric acids, allowing for the formation of enantioenriched homoallylic, propargylic, and crotylic alcohols (up to >99% enantiom

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