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13266-02-9

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13266-02-9 Usage

Chemical Properties

White Solid

Uses

Wittig Reagents.

Check Digit Verification of cas no

The CAS Registry Mumber 13266-02-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,6 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13266-02:
(7*1)+(6*3)+(5*2)+(4*6)+(3*6)+(2*0)+(1*2)=79
79 % 10 = 9
So 13266-02-9 is a valid CAS Registry Number.

13266-02-9SDS

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 (n-tridecyl)triphenylphosphonium bromide

1.2 Other means of identification

Product number -
Other names Triphenyltridecylphosphonium Bromide

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:13266-02-9 SDS

13266-02-9Relevant articles and documents

Method for synthesizing Micromelalopha troglodyta sex pheromone active ingredient

-

, (2020/02/14)

The invention relates to the technical field of insect sex pheromone component synthesis, and provides a novel method for synthesizing Micromelalopha troglodyta sex pheromone active ingredient. According to the novel method, 1, 13-tridecanol is used as an

Total synthesis of N,O,O,O-tetraacetyl-d-ribo-phytosphingosine and its 2-epi-congener

Martinkova, Miroslava,Pomikalova, Kvetoslava,Gonda, Jozef

, p. 84 - 91,8 (2020/08/24)

Total synthesis of the natural d-ribo-phytosphingosine I and its 2-epimer III in the protected form was achieved through a common strategy. The aza-Claisen rearrangement of allylic thiocyanate (Z)-V incorporated the new stereogenic centre with nitrogen and the subsequent Wittig olefination constructed a non-polar side chain. Hydrogenation, followed by removal of protecting groups, completed the syntheses of I and III.

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