아지도아세트산메틸에스테르

Methyl 2-azidoacetate

HCID 4020482CAS 1816-92-8

기본 정보

표준 SMILES
COC(=O)CN=[N+]=[N-]
InChIKey
RXYCUKSOYJWGPE-UHFFFAOYSA-N
분자식
C3H5N3O2
평균 분자량
115.09 g/mol
단동위원소 질량
115.0381764

이름 및 식별자

우선 이름
Methyl 2-azidoacetate
IUPAC
methyl 2-azidoacetate
현지명
아지도아세트산메틸에스테르
영어명
Azidoacetic acid methyl ester
분자식
C3H5N3O2
분자량
115.0907

이름 및 동의어

Methyl 2-azidoacetate1816-92-8DTXSID70398587RefChem:1089321DTXCID00349446Methyl azidoacetateMETHYLAZIDOACETATEMFCD01311034Acetic acid, 2-azido-, methyl estermethyl 3-diazo-3-azaprop-3-enoateAzidoacetic acid methyl esterAcetic acid, azido-, methyl ester
이름 더 보기
아지도아세트산메틸에스테르Methyl 2-azidoacetate 97%Methyl Azido Acetate-BulkMethyl 2-azidoacetate - M34612-Azido-acetic acid Methyl ester
azido-acetic acid methyl esterAzidoacetic acid, methyl estermethyl azido acetatemethyl azido-acetatemethyl-2-azidoacetateMethyl 2-azidoacetate, 97%SCHEMBL13482799SBB001917

데이터베이스 식별자

CAS
1816-92-8
PubChem CID
4020482
DTXSID
DTXSID70398587
EC Number
687-878-4
Nikkaji
J1.247.582I

물성

구조 계산 물성

XLogP
1.2
극성 표면적
40.7 Ų
수소 결합 공여자 수
0
수소 결합 수용자 수
4
회전 가능 결합 수
3
무거운 원자 수
8

물리화학적 성질

끓는 점
35 °C · 35 °C
밀도
1.182 g/mL · 1.182 g/mL at 25 °C
굴절률
20 · n20/D1.440
인화점
48 ℃ · 48℃
물리적 상태
liquid
InChI
InChI=1S/C3H5N3O2/c1-8-3(7)2-5-6-4/h2H2,1H3

안전 및 규제

GHS 분류

GHS Classification · 4건

Warning

H226 (100%): Flammable liquid and vapor [Warning Flammable liquids]

P210, P233, P240, P241, P242, P243, P261, P264, P264+P265, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 39 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

유해성 정보

Hazard Classes and CategoriesFlam. Liq. 3 (100%)

안전 데이터

wgk
3
ridadr
UN 1993C 3 / PGIII
risk_code
5-10-36/37/38
hazard_code
Xi
safety_code
26
위험 등급
3

화학 및 산업

응용 분야 · 1건

용도Methyl 2-azidoacetate is widely used as a precursor to build triazole derivatives via alkyne-azide click chemistry. Some of the examples include the synthesis of coumarin-triazole derivatives as potential antiplasmodial agents and macrocyclic triazole containing largazole analogs as histone deacetylases-1 (HDAC1) inhibitors.It can be used to synthesize various pyrrole derivatives by Knoevenagel condensation as in the synthesis of near-infrared boron dipyrromethene (BODIPY) donors for organic tandem solar cells.It can also be used in Hemetsberger-Knittel synthesis of substituted 5-, 6-, and 7-azaindoles.Synthesis of highly fluorescent pyreno[2,1-b]pyrroles using methyl 2-azidoacetate as one of the reagents.

공급사50 곳

武汉英诺医药科技有限公司+86-027-59232304 15387063101 · [email protected]
上海麦克林生化科技股份有限公司021-50706066 15221275939 · [email protected]
合肥翰刚医药科技有限公司+8618062405514 · [email protected]
韶远科技(上海)有限公司021-50795510 4000665055 · [email protected]
上海凯曼化工科技有限公司021-021-50400622 15618790390 · [email protected]

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