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Benzenemethanol, 2,6-dimethyl-3-nitro-, acetate (ester) is a chemical compound derived from benzenemethanol, which is a type of alcohol containing a benzene ring. This specific compound features two methyl groups (CH3) at the 2nd and 6th positions of the benzene ring, and a nitro group (NO2) at the 3rd position. The acetate (ester) functional group is attached to the hydroxyl group (OH) of the benzenemethanol, forming an ester linkage. Benzenemethanol, 2,6-dimethyl-3-nitro-, acetate (ester) is characterized by its unique chemical structure, which may have potential applications in various fields such as pharmaceuticals, agrochemicals, or as intermediates in organic synthesis.

82617-30-9

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82617-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82617-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,6,1 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82617-30:
(7*8)+(6*2)+(5*6)+(4*1)+(3*7)+(2*3)+(1*0)=129
129 % 10 = 9
So 82617-30-9 is a valid CAS Registry Number.

82617-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,6-dimethyl-3-nitrophenyl)methyl acetate

1.2 Other means of identification

Product number -
Other names 1-acetoxymethyl-2,6-dimethyl-3-nitrobenzene

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:82617-30-9 SDS

82617-30-9Relevant academic research and scientific papers

Quinoline derivatives as bradykinin agonists

-

, (2008/06/13)

PCT No. PCT/JP97/00233 Sec. 371 Date Aug. 3, 1998 Sec. 102(e) Date Aug. 3, 1998 PCT Filed Jan. 31, 1997 PCT Pub. No. WO97/28153 PCT Pub. Date Aug. 7, 1997This invention relates to a compound of formula (1) wherein R1 is halogen, etc., R2 is halogen, etc., R3 is amino substituted with substituent(s) selected from the group consisting of lower alkyl and acyl, etc., R4 is heterocyclic (lower)alkyl, R5 is lower alkyl, and A1 is lower alkylene, and pharmaceutically acceptable salts thereof, to processes for preparation thereof, to a pharmaceutical composition comprising the same, and to methods of using the same therapeutically in the prevention and/or the treatment of hypertension or the like.

A novel class of orally active non-peptide bradykinin B2 receptor antagonists. 3. Discovering bioisosteres of the imidazo[1,2-a]pyridine moiety

Abe, Yoshito,Kayakiri, Hiroshi,Satoh, Shigeki,Inoue, Takayuki,Sawada, Yuki,Inamura, Noriaki,Asano, Masayuki,Aramori, Ichiro,Hatori, Chie,Sawai, Hiroe,Oku, Teruo,Tanaka, Hirokazu

, p. 4062 - 4079 (2007/10/03)

Recently we reported on overcoming the species difference of our first orally active non-peptide bradykinin (BK) B2 receptor antagonists, incorporating an 8-[[3-(N-acylglycyl-N-methylamino)-2,6-dichlorobenzyl]oxy]- 3-halo-2-methylimidazo[1,2-α]

Insecticidal (1,1'-biphenyl)-3-ylmethyl esters

-

, (2008/06/13)

[1,1'-Biphenyl]-3-ylmethyl pyrethroid esters, as well as processes, uses, and intermediates thereto, are disclosed. The [1,1'-biphenyl]-3-ylmethyl pyrethroid esters control a broad spectrum of insects as well as acarids.

Insecticidal [1,1'-biphenyl]-3-ylmethyl esters

-

, (2008/06/13)

[1,1'-Biphenyl]-3-ylmethyl pyrethroid esters, as well as processes, uses, and intermediates thereto, are disclosed. The [1,1'-biphenyl]-3-ylmethyl pyrethroid esters control a broad spectrum of insects as well as acarids.

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