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1266728-07-7

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1266728-07-7 Usage

Derivative

It is a derivative of methanesulfonic acid.

Usage

Primarily used as a reagent in organic synthesis, especially in protecting alcohols and amines.

Physical State

Clear, colorless liquid.

Odor

Faint odor.

Solubility

Soluble in many organic solvents.

Industries

Mainly employed in pharmaceutical and chemical industries.

Versatility

Acts as a versatile intermediate in the synthesis of various compounds.

Stability

Considered relatively stable.

Toxicity

Exhibits low toxicity.

Applications

Widely utilized in laboratory settings.

Check Digit Verification of cas no

The CAS Registry Mumber 1266728-07-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,6,7,2 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1266728-07:
(9*1)+(8*2)+(7*6)+(6*6)+(5*7)+(4*2)+(3*8)+(2*0)+(1*7)=177
177 % 10 = 7
So 1266728-07-7 is a valid CAS Registry Number.

1266728-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dimethylbenzyl methanesulfonate

1.2 Other means of identification

Product number -
Other names -

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:1266728-07-7 SDS

1266728-07-7Downstream Products

1266728-07-7Relevant articles and documents

RENIN INHIBITORS

-

, (2011/04/13)

Renin inhibitors, which are spirocyclic piperidine amides, of structural formula (I) and pharmaceutical compositions thereof useful in the treatment of cardiovascular diseases and renal insufficiency, wherein n, for each instance in which it occurs, is independently 0, 1, or 2; R1 is hydrogen, C1-6 -alkyl or C3-6 -cycloalkyl, wherein said C1-6 -alkyl or C3-6 -cycloalkyl group can be independently substituted with 1-3 halogens; A is (i) a five- or six-membered saturated or unsaturated heterocyclic or carbocyclic monocyclic ring or (ii) a five- or six-membered saturated or unsaturated heterocyclic or carbocyclic ring which is fused to another five- or six-membered saturated or unsaturated heterocyclic or carbocyclic ring, V is a bond or -(C=O)-, -CH(OH)-, -CH2- or =CH-; U is a bond or -CH2-, or for the case when V is =CH-, U is -CH=; X is =CH-, =CF-, =C(OR3)-, or -C=O-; and Y is =CH-, =CF-, =N-, or for the case when X is -C=O-, Y is -N(R3)-.

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