CAS: 1335-66-6; 2,4,6-Trimethylcyclohex-3-Ene-1-Carbaldehyde--3,5,6-Trimethylcyclohex-3-Ene-1-Carbaldehyde (1/1)

英文名称2,4,6-Trimethylcyclohex-3-Ene-1-Carbaldehyde--3,5,6-Trimethylcyclohex-3-Ene-1-Carbaldehyde (1/1)
中文名称2,4,6-三甲基-3-环己烯-1-甲醛
IUPAC名称2,4,6-trimethylcyclohex-3-ene-1-carbaldehyde--3,5,6-trimethylcyclohex-3-ene-1-carbaldehyde (1/1)
其它别名Xene; 3,5,6-Trimethylcyclohex-3-Enecarbaldehyde; Isocyclocitral; 3-Cyclohexene-1-Carboxaldehyde, 2,4,6-Trimethyl; 1-Formyl-3,5,6-Trimethyl-3-Cyclohexene And 1-Formyl-2,4,6-Trimethyl-3-Cyclohexene; 1-Formyl-3,5,6-Trimethyl-3-Cyclohexeneand1-Formyl-2,4,6-Trimethyl-3-Cyclohe; 3-Cyclohexene-1-Carboxaldehyde, 2,4,6-Trimethyl-, And 3,5,6-Trimethyl-3-Cyclohexene-1-Carboxaldehyde
CAS编号1335-66-6
MFCD编号:MFCD00466861
EINECS号:215-638-7
FDA UNII编号:3RP77Q40LC
分子式:C20H32O2
分子量:304.47
产品CID: 506136
产品分类香精与香料 → 合成香料 → 醛类香料 → 脂环醛

相似结构搜索
InChIKey: AEXLFXYEFLKADK-UHFFFAOYSA-N
InChI=1S/2C10H16O/c1-7-4-8(2)9(3)10(5-7)6-11;1-7-4-8(2)10(6-11)9(3)5-7/h2*4,6,8-10H,5H2,1-3H3…
计算化学: 氢键受体数2.0氢键供体数0.0可旋转键数2.0

MSDS等安全信息

GHS象形图
GHS符号GHS07;
注释: Exclamation mark
危险类别皮肤腐蚀/刺激类别2
严重眼刺激类别2
皮肤致敏类别1B
水生慢性毒性类别3
皮肤致敏类别1
警示词Warning(警告)
危险描述H315 |造成皮肤刺激.
H319 |造成严重眼刺激.
H317 |可能引起皮肤过敏反应.
H412 |对水生生物有害并具有长期持续影响.
防范说明P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P-P273-P501-P261-P272-P280-P302+P352-P333+P313-P321-P363-P501

欧盟法规

统一分类与标签ECHA物质ECHA物质C&L通报REACH预注册

合成工艺路线路线简述

海关参考信息

2901210000-乙烯
2901220000-丙烯
2912110000-甲醛
2912120000-乙醛
💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
详情请参考：📖 海关编码查询和海关进出口税则

专利信息

专利号:WO-8911536-A1
优先权日:1988-05-27
标题:Microbial biocatalyst for production of terpenic aldehydes
发明人：DAVIS KAREN JOHANNA; BEST DAVID JOHN; BURFIELD ANTHONY GRAHAM; TAYLOR FRANK; TALBOT JANE STELLA
权利人:NOVALAL LTD
摘要:An active biocatalyst for converting alpha-pinene epoxide to terpenic aldehydes useful in perfumery, e.g. formula (I), is produced by growing a microorganism, preferably Pseudomonas fluorescens NCIB 40043, to late log phase in a medium containing carbohydrate (e.g. glucose) as the carbon source, and adding alpha-pinene. The resulting culture comprises active biocatalyst which is brought into contact with alpha-pinene epoxide for aldehyde synthesis.