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62108-18-3

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62108-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62108-18-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,0 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62108-18:
(7*6)+(6*2)+(5*1)+(4*0)+(3*8)+(2*1)+(1*8)=93
93 % 10 = 3
So 62108-18-3 is a valid CAS Registry Number.

62108-18-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxypent-3-yne

1.2 Other means of identification

Product number -
Other names 5-Methoxy-pent-2-yne

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:62108-18-3 SDS

62108-18-3Downstream Products

62108-18-3Relevant articles and documents

Ring-size ans Substituent Effects in Intramolecular Reactions of Alkylidenecarbenes (Carbenoids)

Baird, Mark S.,Baxter, Anthony G. W.,Hoorfar, Alireza,Jefferies, Ian

, p. 2575 - 2582 (2007/10/02)

Intramolecular reaction of methylenecarbenes (carbenoids), derived by reaction of 1,1-dibromoalkenes and methyllithium, with 5,6-related C-H bonds leads to cyclopentenes when there is an alkoxy or amino substituent on C-5, but no reaction occurs at a 4,5-related C-H bond when there is a heteroatom on C-4; when there is an alkylthio group either on C-4 or C-5 attack occurs on sulphur and the alkyl group is lost, leading to a 2,3-dihydrothiophene or a 3,4-dihydro-2H-thiopyran respectively.If a heteroatom-hydrogen bond is present at the 5,6-position a formal insertion occurs at that bond leading to 2,3-dihydropyrroles, 2,3-dihydrofuranes or 2,3-dihydrothiophenes.

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